Comparative Evaluation of Clinical and Radiographic Treatment Outcomes of Garlic Gel and Calcium Hydroxide as an Intracanal Medicament in Nonsurgical Root Canal Treatment of Permanent Teeth.

Trial statusNot yet recruiting
Trial phasePhase 3
Trial typeInterventional
Biological sexAll
Age15-45
SponsorUniversity of Health Sciences Lahore

About this trial

Researchers want to check how well garlic works inside permanent teeth as a medicament during root canal treatments. Garlic has shown to possess many helpful properties, like reducing inflammation, helping wounds heal, and antimicrobial characteristics. Because conventional medicaments can be expensive or have potential side effects, researchers are actively exploring natural options like garlic. Some lab studies have already shown that garlic gel can kill the microbes inside the teeth. However, no real-life clinical or X-ray studies have been done on using garlic in permanent teeth. This study may help scientists find a much safer and effective new material for dental treatments in the future.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Patients with the physical status of ASA I and ASA II according to ASA classification.

Patients aged from 15-45 years.

Mature permanent single-rooted teeth with closed apices.

Patients with clinical signs of symptomatic apical periodontitis (pain, tenderness to palpation, and percussion).

Disqualifiers

Patients with physical status of ASA III, IV, and V according to ASA classification.

Teeth with a calcified pulp chamber in periapical radiography.

Patients who have undergone previous endodontic treatment failure and those with the presence of sinus tract on clinical examination.

Teeth having advanced periodontal disease, with the basic periodontal examination (BPE) of 3 and 4.

Trial design

Design model

Parallel

Treatments tested in this trial

  • Allium Sativum as an intracanal medicament

    Drug

    Patients will receive informed consent, clinical exam, and preoperative radiographs. After anesthesia and rubber dam isolation, access, cleaning, and shaping of canals will be performed using standard endodontic techniques. A sterile paper point will be placed in the canal for pH evaluation, followed by placement of garlic gel with lentulo spiral and temporary restoration of MD Temp and GC Gold Label 2 GIC. Patients will return after 14 days; if symptoms persist, the medicament will be replaced, and the patient will be reviewed again after 14 days and then after one month. Final obturation will only be done once all symptoms have resolved. If the experimental group continues to show symptoms after three dressings, the case will be considered a failure and treated conventionally. When asymptomatic, the medicament will be removed, canals will be irrigated, dried, obturated with gutta-percha and Endoplus sealer. Radiographic outcomes will be evaluated after 6 months by 2 endodontists.

Treatment groups

96 Participants
are divided into 2 treatment groups
Group A: Experimental group(n=48)Experimental treatment 1 intervention
Group B: Control group(n=48)Active comparator 1 intervention

Trial outcomes

Primary outcomes

1

CLINICAL AND RADIOGRAPHIC OUTCOMES

Clinical success will be based on the absence of the following clinical signs and symptoms: Pain Tenderness to palpation of adjacent soft tissues Tenderness to percussion of involved tooth Radiographic outcomes will be measured in terms of size of Periapical radiolucency. The Periapical status will be assessed using the periapical index (PAI) scoring system by Orstavik. Each tooth will be assigned one of the Periapical index scores for 5 categories within the scale. SCORE POSSIBLE OUTCOME 1. Normal periapical structure 2. Small changes in bone structures 3. Change in bone structure with mineral loss 4. Periodontitis with well-defined radiolucency 5. Severe periodontitis with exacerbating features Periapical radiolucency will be classified as resolved if the Periapical index score is less than or equal to score of 2.

Time frame
Time frame for clinical outcomes: Baseline to 2 weeks Time frame for radiographic outcomes: Baseline to 6 months

Secondary outcomes

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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