Vitamin C for the Prevention of UTI in Women Who Undergo Elective GYN Surgeries
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|ClinicalTrials.gov Identifier: NCT03800667|
Recruitment Status : Withdrawn (No funds)
First Posted : January 11, 2019
Last Update Posted : July 15, 2019
|Condition or disease||Intervention/treatment||Phase|
|Catheter-Associated Urinary Tract Infection, Ascorbic Acid||Drug: Ascorbic Acid 1000 MG||Early Phase 1|
|Study Type :||Interventional (Clinical Trial)|
|Actual Enrollment :||0 participants|
|Intervention Model:||Parallel Assignment|
|Masking:||None (Open Label)|
|Official Title:||Vitamin C for the Prevention of UTI in Women Who Undergo Elective GYN Surgeries: a Study Protocol for a Randomized Controlled Trial|
|Actual Study Start Date :||August 8, 2018|
|Actual Primary Completion Date :||July 12, 2019|
|Actual Study Completion Date :||July 12, 2019|
Experimental: Women on a vitamin C regimen
Women who are undergoing elective gynecological surgeries and who are randomized to take 1000 mg of vitamin C for one month,
Drug: Ascorbic Acid 1000 MG
1000 mg ascorbic acid (Vitamin C) for 1 month post-op after an elective gynecological surgery.
No Intervention: Women not taking vitamin C
Women who are undergoing elective gynecological surgeries and who are randomized not to take any vitamin C for one month.
- Proportion of participants who experienced clinically diagnosed and treated UTI. [ Time Frame: 30 days ]Urinary tract infection is diagnosed by a positive urine culture.
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03800667
|American University of Beirut Medical Center|
|Principal Investigator:||Tony Bazi, MD||American University of Beirut Medical Center|