Bacterial Colonization

3

Review clinical trials related to Bacterial Colonization. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
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

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

Enteral Nutrition and Colonization Resistance Through Microbiota Modulation in Critically Ill Patients

The goal of this clinical trial is to learn whether enteral nutrition enriched with fiber can influence gut microbiota and improve resistance to colonization with multidrug-resistant bacteria in critically ill patients. The study will also evaluate the safety and clinical outcomes associated with fiber-enriched enteral nutrition. The main questions it aims to answer are: * Does fiber-enriched enteral nutrition reduce the acquisition of colonization with multidrug-resistant bacteria during intensive care unit (ICU) hospitalization? * Does fiber-enriched enteral nutrition modify the composition and diversity of the intestinal microbiota? * Are there differences in clinical outcomes, including adverse events, between patients receiving fiber-enriched and non-fiber enteral nutrition? Researchers will compare patients receiving fiber-enriched enteral nutrition with patients receiving standard enteral nutrition without added fiber to determine whether fiber supplementation influences gut microbiota and colonization resistance. Participants will: * Receive enteral nutrition through a feeding tube according to their clinical needs. * Receive either a fiber-enriched enteral nutrition formula or a standard enteral nutrition formula. * Have stool samples collected during ICU hospitalization for analysis of intestinal microbiota and detection of multidrug-resistant bacteria. * Be monitored for clinical outcomes, infections, antibiotic exposure, and adverse events during their ICU stay and follow-up period.

Participants needed: 60
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Iuliu Hatieganu University of Medicine and PharmacyUpdated: Jul 22, 2026Locations: 1
Eligibility criteria

Patients with medical (non-surgical) conditions admitted to the ICU. [+3]

Surgical ICU patients. [+3]