Clinical trials

106

Search and review clinical trials. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Endothelial Markers and Tadalafil Response

This prospective cohort study will recruit eligible men attending the Urology/Andrology outpatient clinic. Baseline assessment will include demographic and clinical data, cardiovascular risk assessment, erectile-function questionnaires, routine laboratory investigations, brachial artery flow-mediated dilatation, carotid intima-media thickness, and selected circulating endothelial biomarkers including endothelin-1, nitrite/nitrate, high-sensitivity C-reactive protein, soluble vascular cell adhesion molecule-1, and soluble intercellular adhesion molecule-1. All participants will receive tadalafil 5 mg once daily for 12 weeks. Erectile function, adherence, and adverse events will be assessed during follow-up. The primary outcome will be clinical response at 12 weeks, defined as an improvement of at least 4 points in the IIEF-EF domain together with a positive response to the Global Assessment Question.

Participants needed: 120
Trial details
Age: 30-70Biological sex: MaleType: ObservationalSponsor: Al-Azhar UniversityUpdated: Aug 20, 2026Locations: 1
Eligibility criteria

Men aged 30 to 70 years. [+8]

ED primarily attributed to psychogenic causes. [+18]

Status: Recruiting

Role of Pre-stenting Before Retrograde Intrarenal Surgery With Miniaturized Flexible Ureteroscopes

This prospective randomized controlled trial will compare retrograde intrarenal surgery performed after routine preoperative ureteral stenting with direct retrograde intrarenal surgery without planned preoperative stenting in adults with unilateral renal calculi measuring 10-20 mm. The study will evaluate stone-free rate, ureteral access, need for rescue stenting, operative outcomes, complications, staged procedures, postoperative recovery, and auxiliary treatment.

Participants needed: 270
Trial details
Age: 18-70Biological sex: AllType: InterventionalSponsor: Al-Azhar UniversityUpdated: Aug 21, 2026Locations: 1
Eligibility criteria

Adults aged 18-70 years. [+7]

Bilateral renal calculi requiring simultaneous surgical treatment. [+14]

Status: Not yet recruiting

Bedtime Device Restriction and Desmopressin in PMNE.

This randomized controlled trial will evaluate whether restricting bedtime digital-device use improves the response to desmopressin in children with primary monosymptomatic nocturnal enuresis. Participants will receive desmopressin for 8 weeks and will be assigned to either bedtime device restriction or usual screen habits.

Participants needed: 140
Trial details
Age: 6-14Biological sex: AllType: InterventionalSponsor: Al-Azhar UniversityUpdated: Aug 20, 2026Locations: 1
Eligibility criteria

Age 6-14 years. [+4]

Secondary enuresis or non-monosymptomatic enuresis (daytime incontinence, urgenc... [+4]

Status: Recruiting

Long-term Safety of UAS-assisted vs Sheathless RIRS in Non-prestented Patients

This retrospective comparative cohort study will include adult patients who underwent primary RIRS for renal stones ≤20 mm at Al-Azhar University Hospitals between January 2020 and December 2025. Patients will be classified by whether a ureteral access sheath (UAS) was used during the index RIRS, and all eligible patients will be invited for active long-term follow-up (minimum 12 months) to assess the composite outcome of delayed ipsilateral ureteral stricture or new/progressive ipsilateral hydronephrosis and other safety and efficacy outcomes. Propensity-score methods and adjusted regression analyses will be used to control confounding.

Participants needed: 1,200
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Al-Azhar UniversityUpdated: Aug 18, 2026Locations: 1
Eligibility criteria

Age ≥18 years at time of index RIRS. [+6]

Primary ureteral stone treated during the same procedure. [+6]

Status: Recruiting

Risk Factors and Clinical Implications of Double-J Ureteral Stent Bacterial Colonization

This prospective cohort study will evaluate the risk factors associated with bacterial colonization of Double-J ureteral stents and examine its clinical implications. Adult patients undergoing temporary ureteral stent insertion for routine urological indications will be followed until stent removal, when urine and stent cultures will be obtained. The study will assess the association between colonization and factors such as indwelling time, diabetes mellitus, chronic kidney disease, prior urinary tract infection, prior antibiotic exposure, and stent-related symptoms.

Participants needed: 300
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Al-Azhar UniversityUpdated: Aug 18, 2026Locations: 1Duration: 48 Weeks
Eligibility criteria

Age 18 years or older. [+5]

Active urosepsis at insertion. [+6]

Status: Recruiting

Daily Tadalafil as Adjunctive Therapy Versus Monotherapy for PDE5 Inhibitor-Resistant Erectile Dysfunction

This randomized trial will compare daily tadalafil 5 mg as adjunct therapy versus monotherapy in men with on-demand PDE5 inhibitor-resistant erectile dysfunction. The study will evaluate changes in erectile function, treatment satisfaction, partner satisfaction, and safety over 12 weeks.

Participants needed: 260
Trial details
Phase: Phase 4Age: 18-70Biological sex: MaleType: InterventionalSponsor: Al-Azhar UniversityUpdated: Aug 18, 2026Locations: 1
Eligibility criteria

Age: 18 to 70 years. [+6]

Current use of nitrates. [+8]

Status: Recruiting

Flexible Nephroscopy-Assisted Single-Tract Versus Multi-Tract Percutaneous Nephrolithotomy for Complex Renal Stones

This randomized, parallel-group, non-inferiority trial will compare flexible nephroscopy-assisted single-tract percutaneous nephrolithotomy with conventional multi-tract percutaneous nephrolithotomy in patients with complex unilateral renal stones. The primary outcome is stone-free rate at 3 months, and secondary outcomes include operative time, fluoroscopy time, hemoglobin drop, transfusion rate, hospital stay, complications, need for auxiliary procedures, and cost-effectiveness.

Participants needed: 470
Trial details
Age: 18-70Biological sex: AllType: InterventionalSponsor: Al-Azhar UniversityUpdated: Aug 18, 2026Locations: 1
Eligibility criteria

Age 18-70 years.

Status: Recruiting

Lifestyle Modification for Erectile Dysfunction in Men With Metabolic Syndrome

Metabolic syndrome is associated with erectile dysfunction through obesity, insulin resistance, abnormal blood lipids, high blood pressure, and impaired blood-vessel function. This study will evaluate whether a structured six-month lifestyle-modification program can improve penile blood flow and erectile function in men with metabolic syndrome-associated erectile dysfunction. Eligible participants will receive dietary counseling, exercise guidance, weight-management advice, smoking-cessation counseling when applicable, sleep and sedentary-behavior advice, and repeated behavioral reinforcement. Erectile function, penile blood-flow measurements obtained by penile duplex Doppler ultrasonography, body measurements, and selected metabolic laboratory parameters will be assessed before the program and after six months.

Participants needed: 55
Trial details
Age: 30-65Biological sex: MaleType: InterventionalSponsor: Al-Azhar UniversityUpdated: Aug 14, 2026Locations: 2
Eligibility criteria

Men aged 30-65 years. [+6]

Erectile dysfunction primarily attributable to neurogenic, psychogenic, hormonal... [+11]

Status: Not yet recruiting

Acceptance and Commitment Therapy Plus Physiotherapy for Chronic Low Back Pain

This study is a randomized controlled trial (RCT) investigating whether adding Acceptance and Commitment Therapy (ACT) to standard physiotherapy provides greater benefits for adults with chronic low back pain than physiotherapy alone. A total of 60 participants will be randomly allocated into two groups: ACT plus physiotherapy and physiotherapy alone. Both groups will receive a 8-weeks program with two sessions per week. The ACT component focuses on acceptance, psychological flexibility, mindfulness, cognitive defusion, values, and committed action. The main outcomes are pain catastrophizing, functional disability, perceived stress, and sleep quality, assessed using the PCS, ODI, PSS, and PSQI. The study aims to determine whether combining psychological and physical rehabilitation produces better outcomes than physiotherapy alone.

Participants needed: 64
Trial details
Age: 18-55Biological sex: AllType: InterventionalSponsor: Al-Azhar UniversityUpdated: Aug 14, 2026
Eligibility criteria

Not listed

Status: Not yet recruiting

Efficacy and Safety Of Fractional Carbon Dioxide Laser Plus Topical Metformin In Treatment Of Acanthosis Nigricans

evaluate and compare the clinical Efficacy \& Safety Of Fractional Carbon Dioxide (Co₂) Laser Plus Topical Metformin In Treatment Of Acanthosis Nigricans.

Participants needed: 34
Trial details
Phase: Phase 1Age: 18-50Biological sex: AllType: InterventionalSponsor: Al-Azhar UniversityUpdated: Aug 12, 2026
Eligibility criteria

- male or female patients aged 18-50 years [+4]

- pregnancy or lactation [+6]

Status: Not yet recruiting

Clinical and Radiographic Evaluation of Low Sagittal Medial Ramus Osteotomy for Treatment of Skeletal Class II and Class III Malocclusion

This prospective clinical trial aims to evaluate the clinical and radiographic outcomes of the low sagittal medial ramus osteotomy-a technical modification of the conventional sagittal split osteotomy (SSO)-for treating patients with skeletal Class II and Class III malocclusions. Standard sagittal split osteotomies carry risks of complications, including unfavorable osteotomy propagation (bad splits) toward the condyle, ramus fragmentation, lingual interference of the distal segment, and inferior alveolar nerve (IAN) injury. To minimize these risks, this study utilizes a modified medial cut positioned low (below the lingula in an area with adequate marrow space) and short (terminating anterior to the lingula). This design aims to prevent osteotomy extension into the condylar region and eliminate lingual interference during segment repositioning.

Participants needed: 11
Trial details
Age: 18-45Biological sex: AllType: InterventionalSponsor: Al-Azhar UniversityUpdated: Aug 5, 2026
Eligibility criteria

Patients with skeletal Class II or Class III malocclusion requiring mandibular o... [+2]

Patients with a pre-existing history of inferior alveolar nerve (IAN) sensory im... [+3]

Status: Recruiting

Nailfold Capillaroscopic Changes in Psoriasis

The goal of this observational study is to evaluate nailfold capillaroscopic changes in patients with psoriasis and to assess their correlation with disease severity. The study will also explore differences in capillaroscopic findings across different clinical types of psoriasis and skin phototypes (Fitzpatrick classification). The study will include patients diagnosed with psoriasis attending dermatology outpatient clinics. Participants will undergo clinical assessment and nailfold capillaroscopy to detect microvascular changes.

Participants needed: 100
Trial details
Biological sex: AllType: ObservationalSponsor: Al-Azhar UniversityUpdated: Jul 31, 2026Locations: 1
Eligibility criteria

Patients clinically diagnosed with psoriasis.

Patients with connective tissue diseases (e.g., systemic sclerosis, SLE) [+5]

Status: Recruiting

Risk Factors and Clinical Implications of Double-J Ureteral Stent Bacterial Colonization: A Prospective Cohort Study

To identify the risk factors associated with bacterial colonization of Double-J ureteral stents and to evaluate its clinical implications, including bacteriuria, UTI, antimicrobial resistance, and stent-related symptoms.

Participants needed: 400
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Al-Azhar UniversityUpdated: Aug 3, 2026Locations: 1Duration: 2 Weeks
Eligibility criteria

Patients undergoing temporary Double-J ureteral stent insertion. [+4]

Active urosepsis at the time of stent insertion. [+6]

Status: Not yet recruiting

Low-Intensity Shock Wave Therapy for Refractory Overactive Bladder in Women

Overactive bladder is a condition characterized by a sudden and difficult-to-control need to urinate, which may occur with frequent urination, nighttime urination, and urine leakage. Some women continue to experience these symptoms despite lifestyle changes, behavioral therapy, and medication, or they cannot tolerate or decline medical treatment. This study will evaluate whether low-intensity extracorporeal shock wave therapy (Li-ESWT), a non-surgical treatment delivered externally over the lower abdomen, can safely improve refractory overactive bladder symptoms in women. A total of 40 women will be randomly assigned in equal numbers to receive either active Li-ESWT or a sham treatment. Both groups will attend one treatment session each week for six weeks. The sham procedure will be similar to the active treatment in positioning, session duration, and device sound but will not deliver shock wave energy. Symptoms will be assessed using the validated Arabic version of the 8-item Overactive Bladder Questionnaire (OAB-V8) before treatment and during follow-up. The main purpose of the study is to compare the change in OAB-V8 symptom score between the two groups after one month. Additional assessments at three months will include post-void residual urine volume, information from a 3-day voiding diary, the participant's overall impression of improvement, and any treatment-related adverse events. The study hypothesis is that Li-ESWT will improve overactive bladder symptoms and quality of life compared with sham treatment.

Participants needed: 40
Trial details
Age: 18-70Biological sex: FemaleType: InterventionalSponsor: Al-Azhar UniversityUpdated: Jul 31, 2026Locations: 1
Eligibility criteria

Female participants aged 18 to 70 years. [+3]

Current use of medical treatment for overactive bladder. [+10]

Status: Recruiting

Management of Early Onset Scoliosis by Active Apex Correction Technique

Early onset scoliosis is challenging cases in management .different techniques used to correct the deformity ranging between fusionlees and fusion surgery. Fusionless surgery permits developments of vertebral column and lung to avoid thoracic insufficiency syndrome. Fusion surgeries for complicated and high curves .New fusionless technique that I will use in my research is to modulate and guide the growth of the Apex of deformity through tethering the convex side and modulate the concave side and follow up the patients to see the results on their radiological and clinical parameters.

Participants needed: 15
Trial details
Age: 1-10Biological sex: AllType: InterventionalSponsor: Al-Azhar UniversityUpdated: Jul 27, 2026Locations: 1
Eligibility criteria

patients with early-onset scoliosis below 10 years [+1]

Patients above 10 years. [+1]

Status: Recruiting

Surgical-Clinical Correlation in Unilateral Conductive Hearing Loss With Intact Tympanic Membrane

Unilateral conductive hearing loss (UCHL) in the presence of an intact tympanic membrane represents a diagnostic challenge in otologic practice. In the absence of middle ear effusion or tympanic membrane pathology, stapes fixation secondary to otosclerosis is often considered the most probable diagnosis. However, although otosclerosis is traditionally regarded as a bilateral disease, clinical presentation may be unilateral due to asymmetric disease progression or subclinical contralateral involvement. Other etiologies, including congenital ossicular anomalies, ossicular discontinuity, tympanosclerosis without tympanic membrane involvement, or oval window abnormalities, may mimic otosclerosis both clinically and audiologically. Consequently, exploratory tympanotomy remains the gold standard for definitive diagnosis, allowing direct assessment of ossicular chain mobility and confirmation of stapes fixation. Correlating preoperative clinical suspicion with intraoperative findings is therefore essential to better define the true causes of unilateral conductive hearing loss with an intact tympanic membrane.

Participants needed: 100
Trial details
Biological sex: AllType: InterventionalSponsor: Al-Azhar UniversityUpdated: Jul 24, 2026Locations: 1
Eligibility criteria

unilateral conductive hearing loss or mixed HL with intact Tympanic Membrane [+1]

Sensorineural hearing loss [+3]

Status: Recruiting

Omega-3 Plus Low-Dose Aspirin in Smokers With Stage III Periodontitis

This randomized double-blind placebo-controlled clinical trial aims to evaluate the clinical and biochemical effects of omega-3 fatty acids combined with low-dose aspirin as an adjunct to scaling and root planing (SRP) in smoker patients with Stage III periodontitis. The study compares test and control groups regarding periodontal clinical parameters and gingival crevicular fluid interleukin-1 beta (IL-1β) levels Or other inflammatory markers that will be determined later at baseline, 3 months, and 6 months following treatment

Participants needed: 40
Trial details
Age: 30-50Biological sex: AllType: InterventionalSponsor: Al-Azhar UniversityUpdated: Jul 8, 2026Locations: 1
Eligibility criteria

- Male or female smokers aged 30 to 50 years. [+5]

- Systemic diseases affecting periodontal health. [+7]

Status: Recruiting

Effect of Co-enzyme Q10 and Vitamin C Alone or in Combination After a Surgical Gingival Depigmentation

This study aims to assess the clinical effectiveness of Co-enzyme Q10 and Vitamin C, applied individually or in combination after surgical gingival depigmentation.

Participants needed: 20
Trial details
Age: 18-45Biological sex: AllType: InterventionalSponsor: Al-Azhar UniversityUpdated: Jul 1, 2026Locations: 1
Eligibility criteria

Systemically healthy patient of both genders aged from 18-45 years. [+3]

Patient clinically diagnosed with periodontitis. [+4]

Status: Recruiting

Twin-Block and LIPUS for TMJ Outcomes in Skeletal Class II Patients

Evaluation of the efficacy of early treatment of skeletal class II patients with twin-block in conjunction with low intensity pulsed ultrasound on temporomandibular joint region: a prospective clinical trial

Participants needed: 24
Trial details
Age: 10-14Biological sex: AllType: InterventionalSponsor: Al-Azhar UniversityUpdated: Jun 30, 2026Locations: 1
Eligibility criteria

Skeletal class II due to retrognathic mandible. [+7]

Skeletal class II due to prognathic maxilla. [+5]

Status: Not yet recruiting

Pupillary Light Reflex to Predict Post-Spinal Hypotension in Elective Cesarean Delivery

This prospective observational cohort study investigates whether pre-anesthetic pupillary light reflex (PLR) parameters can predict the risk of hypotension following spinal anesthesia in women undergoing elective cesarean section. Spinal anesthesia-induced hypotension is common, with reported incidence rates of 50-90%, and current predictors such as baseline blood pressure and BMI have limited accuracy. PLR, a sensitive marker of autonomic nervous system balance, may offer a simple, objective, and non-invasive tool for identifying patients at higher risk. The study evaluates pupillary reaction latency and other PLR parameters and correlates them with post-spinal blood pressure changes to determine their predictive value.

Participants needed: 200
Trial details
Age: 18-45Biological sex: FemaleType: ObservationalSponsor: Al-Azhar UniversityUpdated: Jul 1, 2026
Eligibility criteria

Not listed

Status: Not yet recruiting

NCMT Technique and Jodhpur Technique and Excimer Laser in Treatment of Non Vitiligo Leucoderma

This study aims to compare the efficacy and safety of Melanocyte Keratinocyte Transplantation Procedure (MKTP) combined with 308-nm excimer laser versus Jodhpur technique combined with 308-nm excimer laser in the treatment of stable non-vitiligo leukoderma. Twenty-two patients with stable depigmented lesions will be enrolled. In each patient, two comparable lesions will be treated using different techniques. Clinical outcomes including percentage of repigmentation, color match, time to onset of repigmentation, complications, and histological changes will be assessed during follow-up to determine the optimal surgical treatment approach for non-vitiligo leukoderma.

Participants needed: 22
Trial details
Age: 18-60Biological sex: AllType: InterventionalSponsor: Al-Azhar UniversityUpdated: Jun 23, 2026
Eligibility criteria

Age 18 to 60 years. [+5]

Vitiligo or suspected active vitiligo. [+7]

Status: Not yet recruiting

Bilogical Assesment During Intrusion of Lower Incisors

biological assesment during intrusion of lower incisors

Participants needed: 16
Trial details
Age: 14-18Biological sex: AllType: InterventionalSponsor: Al-Azhar UniversityUpdated: Jun 16, 2026
Eligibility criteria

Patients requiring extraction-based orthodontic treatment [+4]

Systemic diseases affecting bone metabolism [+4]

Status: Recruiting

Erythropoietin Gel Effect on Dental Implant Stability

* Achieving and maintaining long-term osseointegration for dental implants is a key objective in the field of dentistry. The success of osseointegration is influenced by the surface treatment applied to dental implants. Numerous coating techniques have been developed to improve and speed up osseointegration. * The aim of the current study is to assess immediate dental implant stability coated with erythropoietin gel, both clinically and radiographically. * Materials and Methods: We conducted a randomized controlled clinical trial.The sample will include patients demanding immediate implant treatment in the anterior maxilla . Patients will be randomly allocated into the two groups of the study. The group A will be treated with erythropoietin gel coated dental implant immediately after extraction of non restorable teeth in the anterior maxilla . Group B will be treated with non coated dental implant immediately after extraction of non restorable teeth in the anterior maxilla . * The primary outcome variable will be implant stability and the secondary outcome will be crestal marginal bone level and bone density around implants. It will be measured at time of implant placement and reevaluated after 6-months .

Participants needed: 24
Trial details
Age: 20-50Biological sex: AllType: InterventionalSponsor: Al-Azhar UniversityUpdated: May 18, 2026Locations: 1
Eligibility criteria

All patients Should have nonrestorable teeth in the anterior maxilla indicated f... [+1]

Heavy smokers who smoke more than ten cigarettes per day [+5]

Status: Recruiting

The Relation Between Oral Hygiene and Microbial Load in the Oral Cavity After Restoring Primary Molars With Two Types of Ready-made Crowns

Following the restoration of primary molars with stainless steel and bioflex crowns, an evaluation of the current state of oral hygiene in relation to the amount of microorganisms and gingival health in the oral cavity will be carried out.

Participants needed: 40
Trial details
Age: 4-8Biological sex: AllType: ObservationalSponsor: Al-Azhar UniversityUpdated: May 12, 2026Locations: 2
Eligibility criteria

Participants aged between 4 and 8 years. [+3]

Special children with physical disabilities or emotional disturbances. [+3]

Status: Recruiting

Modulation of Periapical Inflammation Following Nano-sized Intracanal Medication. A Randomized Controlled Clinical Trial

The main cause of endodontic disorders is microbial infection. From the infected pulp tissue, microorganisms can penetrate into the deeper layers of root dentine and propagate a periapical tissue through the apical foramen and lateral canals causing apical periodontitis. Apical periodontitis is an inflammatory condition affecting the periapical area of teeth with a global prevalence of 52% among individuals and 5% at tooth level. At the periapical region, microbes and their products encounter the host immune defense. Innate immune cells combat bacteria through phagocytosis and release anti-microbial substances, while adaptive immune cells initiate both cell-mediated and humoral immune responses. This immune activation also stimulates osteoclasts, leading to bone resorption and creating space for the inflammatory cells' infiltration . During periapical inflammation, immune cells migrate to the periapical area, where they release pro-inflammatory cytokines such as tumor necrosis factor-alpha (TNF-α), along with anti-inflammatory cytokines like interleukin-10 (IL-10). These cytokines play crucial roles in modulating inflammation and tissue repair. MicroRNAs (miRNAs) are evolutionarily conserved small (18-22 nucleotides) single-stranded, noncoding RNAs. It has been well acknowledged that miRNAs influence gene expression at the posttranscriptional level by targeting mRNA 3'-untranslated regions (3'-UTRs). Accumulating evidence has suggested that miRNA expression is related to the clinical and biological features of diverse diseases, and they can be potential biomarkers for diagnosis, treatment, and prognosis. miRNAs have revealed their critical roles in regulating various cellular functions, including proliferation, apoptosis, differentiation, metabolism, and tumorigenesis, by targeting specific mRNAs. MiR-146a regulates innate immunity, inflammatory responses, and the antiviral pathway. Changes in miR-146a expression have been noted in many human diseases, including autoimmune disorders and cancers. In addition, miR-146a is an important biomarker of disease diagnosis, prevention, and treatment. It is a negative regulator of inflammatory responses by suppressing target gene expression. However, limited data is available regarding the functional role of miR-146a in modulating the inflammatory response of periapical tissues following root canal disinfection in endodontic retreatment cases. Eliminating microorganisms is the primary objective of root canal therapy in order to create an environment as free of bacteria as possible. However, not all root canal treatments are completely successful, and in some cases, the infection persists leading to development of secondary apical periodontitis in previously treated teeth. Disinfecting the root canal during retreatment is significantly more challenging due to the presence of persistent microorganisms that have settled in the root canal system. These microbes are often resistant to standard irrigations and antimicrobial agents leading to the formation of periradicular lesions. Such bacteria can survive for extended periods around the previously filled root canals. Sodium hypochlorite (NaOCl) is the most widely used irrigant in root canal therapy due to its strong antibacterial effect and its ability to dissolve organic substances. Effective canal cleaning is difficult to achieve without the use of NaOCl at a sufficiently high concentration. However, NaOCl has several drawbacks, including its cytotoxicity which can lead to tissue damage and patient symptoms. Additionally, its strong oxidizing nature negatively affects the mechanical properties of dentin such as microhardness and elastic modulus. NaOCl should be used with caution in endodontic procedures to prevent hypochlorite accidents. Calcium hydroxide (Ca (OH)2) is the most widely utilized intracanal medication. It has the potential to dissolve tissue, acts as a physical barrier and generates hydroxyl ions, creating an extremely alkaline environment. It has been shown to be quite effective in the treatment of teeth with persistent periapical lesions. To provide optimal endodontic treatment, the root canal system should be thoroughly cleaned of soft-tissue debris, smear layer, and bacteria. Nanoparticles (NPs) have unique characteristics such as smaller sizes, increased surface area to volume ratio, and higher chemical reactivity and charge density leading to greater interaction with the environment and negatively charged bacterial cells, compared to their bulk counterparts. These advantages can be used to design highly anti-microbial agents with maximal therapeutic efficacy and minimal side effects.

Participants needed: 63
Trial details
Age: 20-40Biological sex: MaleType: InterventionalSponsor: Al-Azhar UniversityUpdated: May 6, 2026Locations: 1
Eligibility criteria

Not listed