BV Study

Not Applicable

• Conditions: Urological and Genital Diseases; Bacterial vaginosis

• Registration Number: PACTR201804003327269
• Lead Sponsor: Perinatal HIV Research Unit

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2018-04-13
• Last Update Posted: 29 May 2023

Recruitment & Eligibility

• Status: Complete
• Sex: Female
• Target Recruitment: 39

Inclusion Criteria

Females.
18-40 years.
Pre-menopausal on menstrual history.
Read and understand English.
Provide voluntary informed consent.
HIV-negative.
Intact genital tract.
Use Depot Medroxyprogesterone Acetate or norethisterone enanthate injectable contraception for at least 7 days by visit 1 (day 0)
Willing to receive HIV testing and counselling

Exclusion Criteria

Positive for pregnancy test or breastfeeding at study entry.
Infected with C. trachomatis or T. vaginalis.
History of abnormality on Pap test.
Currently using oral contraceptive.
Menstruating on enrollment.
Did not have sexual debut.
Treated with antibiotics within eight weeks of study enrollment.
Using oral or vaginal probiotic capsules within eight weeks of enrollment in the study.

Study & Design

• Study Type: Interventional
• Study Design: Not specified