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NCT06615232Recruiting

The Impact of Vaginal Washing on Cervical Inflammation

The Impact of Vaginal Washing on Cervical Inflammation: A Randomized Controlled Trial

Source: ClinicalTrials.gov · Last updated 5 May 2026

Brief summary (registry, in English)

Vaginal washing is a common practice that many women perceive as hygienic. However, vaginal washing has been linked to adverse reproductive health outcomes including increased HIV acquisition risk. The mechanism linking vaginal washing to HIV risk remains unknown, but may be related to increased inflammation caused by intravaginal washing practices. The primary objective of this study is to test the hypothesis that a vaginal washing cessation intervention will reduce concentrations of soluble inflammatory mediators in cervicovaginal fluid and total immune cells in mucosal tissue, reduce cervical epithelial disruption, and increase concentrations of protective vaginal Lactobacillus spp. compared to control.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
122 (estimated)
First submitted
23 Sept 2024
Start date
16 May 2025
Primary completion date
Oct 2026
Lead sponsor
University of Washington
NCT number
NCT06615232

What you commit to

  • Study type: Interventional
  • Planned participants: 122
  • From 16 May 2025 to the primary completion date, Oct 2026
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • History of bleeding disorder

Other

  • \<3 months postpartum or current breastfeeding
  • Current menstruation (can enroll after menses)
  • Visible cervical abnormality requiring evaluation
  • Medical contraindication to study protocol
  • Visible cervicovaginal ulcers or lesions
  • Positive test for gonorrhea, chlamydia, trichomonas, or wet preparation and examination findings indicating vulvovaginal candidiasis

Who the study is looking for

  • Reports vaginal washing beyond the introitus in the past week
  • Female, aged 18-50
  • Presence of a cervix
  • Informed consent obtained and form signed
  • HIV-seronegative
  • Non-pregnant (urine β-hCG negative)
  • Willing to abstain from sex for 14 days after biopsy
  • Post-menarche and pre-menopause

Age in the registry: 18 years to 50 years · Sex: Female · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Pwani Research Center
Coordinator of this site? Confirm its status
MombasaKenyaRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.