About this trial
Double-blind placebo-controlled randomized trial aiming to assess the role of Vitamin C supplementation in the prevention of catheter-associated urinary tract infections in women undergoing elective gynecological surgeries.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Nonpregnant women
18 years of age or older
Undergoing elective GYN surgery
Disqualifiers
Pregnant women
Already taking Vitamin C supplementation
Nephrolithiasis
Congenital anomaly or neurogenic bladder
Trial design
Parallel
Treatments tested in this trial
Ascorbic Acid 1000 MG
Drug1000mg Ascorbic acid orally daily started on the day of elective gynecological surgery for 10 days
Placebo
DrugPlacebo tablet daily starting day of elective gynecological surgery for 10 days
Treatment groups
Trial outcomes
Primary outcomes
Incidence of UTI
The Primary endpoint is the proportion of participants who experience a clinically diagnosed and treated UTI as evidenced by a positive urine culture.
Secondary outcomes
Asymptomatic UTI
The proportion of participants with a positive urine culture, while asymptomatic (asymptomatic bacteriuria) at the end of the study period
Sponsors and contacts
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American University of Beirut Medical Center
Lead sponsor
Moscow State University of Medicine and Dentistry
Collaborator