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Vitamin C for the Prevention of UTI in Women Who Undergo Elective Gynecological Surgeries

A

American University of Beirut Medical Center

Status and phase

Withdrawn
Early Phase 1

Conditions

Catheter-Associated Urinary Tract Infection, Ascorbic Acid

Treatments

Other: Placebo
Drug: Ascorbic Acid 1000 mg

Study type

Interventional

Funder types

Other

Identifiers

NCT04261036
OGY.TB.09/BIO-2017-0609

Details and patient eligibility

About

This open-label randomized trial aims at assessing the role of Vitamin C pills in the prevention of catheter-associated urinary tract infections in women undergoing elective gynecological surgeries.

Sex

Female

Ages

18 to 90 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Non pregnant women at least 18 years of age visiting the Preadmission unit (PAU) or the OBGYN floor (7N), presenting for elective GYN surgery at the American University of Beirut Medical Center (AUBMC).

Exclusion criteria

  • Any women with the following:

    1. Nephrolithiasis
    2. Congenital anomaly or neurogenic bladder
    3. Allergy to ascorbic acid
    4. Who require therapeutic anticoagulant medicine during the 6 weeks after surgery
    5. Surgery did involve a fistula repair or a vaginal mesh removal
    6. Positive Urinalysis in the PAU
    7. Recurrent UTI's
    8. Diabetes
    9. G6PD
    10. Hemochromatosis
    11. Renal disorders

Patients already taking Vitamin C supplementation will also be excluded from the study.

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Triple Blind

0 participants in 2 patient groups, including a placebo group

Women on a vitamin C regimen
Experimental group
Description:
Women who are undergoing elective gynecological surgeries and who are randomized to take 1g of vitamin C for 14 days.
Treatment:
Drug: Ascorbic Acid 1000 mg
Women on a placebo regimen
Placebo Comparator group
Description:
Women who are undergoing elective gynecological surgeries and who are randomized to take placebo for 14 days
Treatment:
Other: Placebo

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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