WHO ICTRP trial

Fecal microbiota transfer for the secondary prevention of recurrent urinary…

CTIS2025-520452-28-00 · EU Clinical Trials Information System · Not Recruiting

Key facts

Trial ID CTIS2025-520452-28-00
Public title Fecal microbiota transfer for the secondary prevention of recurrent urinary tract infections in premenopausal women: a phase II trial (FEMITRANS)
Scientific title Fecal microbiota transfer for the secondary prevention of recurrent urinary tract infections in premenopausal women: a phase II trial (FEMITRANS) - FEMITRANS
Primary sponsor Goethe University Frankfurt
Registry EU Clinical Trials Information System
Recruitment status Not Recruiting
Study type Interventional clinical trial of medicinal product
Phase Human pharmacology (Phase I): No Therapeutic exploratory (Phase II): Yes Therapeutic confirmatory - (Phase III): No Therapeutic use - (Phase IV): No
Countries Germany
Conditions Recurrent urinary tract infections (rUTI);Therapeutic area: Diseases [C] - Bacterial Infections and Mycoses [C01]
Interventions Product Name: MOVIPREP, Pulver zur Herstellung einer Lösung zum Einnehmen, Product Code:PRD324629, Pharmaceutical Form: ORAL SOLUTION, Other descriptive name: , Strength: , Product Name: VANCOMYCIN, Product Code:SUB05076MIG, Pharmaceutical…
Registration date Mar 24, 2025
Target size 24
Registry page euclinicaltrials.eu

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Source: World Health Organization (WHO), International Clinical Trials Registry Platform (ICTRP) · Source date:

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