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Completed

NCT Number: NCT03414060

Feasibility of the Menstrual Cup for VVF

This study examines the feasibility and acceptability of the vaginal menstrual cup for short-term management of vesicovaginal fistula (VVF) among 11 women seeking treatment at a health facility in Ghana. The repeated measures design utilizes a 2-hr pad test to compare urinary leakage with and without the insertable cup, a questionnaire on acceptability and perceived effect is administered and a clinical exam is completed. Subsequently, semi-structured interviews will be carried out with up to 24 additional women seeking treatment at a health facility in Ghana. Interviews will cover women's experiences of living with fistula, including strategies for coping with urinary incontinence and resulting stigma, as well as user acceptability to the intervention.

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Key information

About this study

Vesicovaginal fistula (VVF) is a debilitating maternal morbidity that largely results from complications of prolonged, obstructed labor when the trapped fetal head applies direct pressure to pelvic/vaginal tissues and causes widespread ischemia, tissue necrosis, and subsequent extensive fistula formation. Women living with VVF, the most common anatomical presentation of obstetric fistula, experience urinary incontinence which causes discomfort, malodor, and skin infection, as well as social and psychological consequences that increase their vulnerability to the negative effects of stigma and reduce their quality of life.

Traditional management requires surgical repair; however, many women either do not have access to surgery, or access is delayed due to various individual, social, or structural barriers. Non-surgical management, previously explored with non-invasive techniques for residual urinary incontinence, has been under-examined for fistula-related urinary incontinence. The menstrual cup may be a useful option for non-surgical management of obstetric fistula. Clinical and programmatic reports suggest a potential translation of the menstrual cup for collection or control of urine leakage in women with VVF; however, evidence has not been collected and examined systematically within a population in an endemic setting.

While surgical management of fistula remains the gold standard in treatment, research on non-surgical therapies is necessary.Therefore, this study aims to assess the feasibility (including efficacy, safety, and acceptability among users) of using the menstrual cup over a short period among women seeking care for VVF in a clinical setting and, unlike prior reports, includes standardized measures of leakage and prioritizes user perspectives.

A repeated measures design compared volume of leakage with the and without the cup to baseline leakage via a 2-hr pad test among women with VVF seeking surgical repair at a health facility in Ghana. A questionnaire was later administered followed by a physical exam. A paired t-test was used to analyze effect.

Beginning October 2018, semi-structured interviews with up to 24 women seeking treatment at a health facility in Ghana will be carried out on women's experience with fistula, including strategies for coping with urinary incontinence and resulting stigma, as well as their acceptability to the insertable device. This mixed methods approach is necessary to compare quantitative results and qualitative findings regarding what women are already doing to cope with incontinence and stigma, and their acceptability to this device to manage leaking and support coping.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patient seeking surgical repair for VVF
  • VVF confirmed by gynecologic examination
  • Adequate vaginal capacity to accommodate the menstrual cup
  • Fistula high in vagina (determined at gynecologic examination)
  • Willingness to insert and remove the device by one's self

Exclusion criteria

  • Technically difficult to insert and or remove the menstrual cup (eg severely scarred vagina)
  • Unable or unwilling to learn to insert and remove the menstrual cup
  • Patient who declines consent or is incapable of consent
  • Presence of rectovaginal fistula (RVF) or combined RVF and VVF
  • Fistula low in the vagina precluding collection of urine by the menstrual cup

Treatment and study plan

Menstrual Cup

Device

Primary outcomes

  1. Volume of urinary leakage (in ml)

    Time frame: Over 2 hours

    Measured by 2-hr pad test

Secondary outcomes

  1. Acceptability of the menstrual cup

    Time frame: Over 2 hours

    Using a Likert scale with values ranging from 1-5, acceptability is reported based on ease of use, insertion, wearing, removal, and cleaning. A summarizing acceptability scale is not reported.

  2. Adverse events

    Time frame: Over 2 hours

    Erythema, edema/induration, erosion, bleeding assessed by clinical exam

  3. Rate of enrollment through study completion

    Time frame: through study completion, an average of 1 year

    Number of individuals who enroll out of the total number of individuals screened

  4. Rate of consent through study completion

    Time frame: through study completion, an average of 1 year

    Number of individuals who complete the consent form out of the total number of screened individuals meeting all other inclusion and exclusion criteria

  5. Perceived assessment of leakage with use of the menstrual cup

    Time frame: After 1 hour of use

    Proportion of participants that perceive a reduction in leakage (either marked or slight) with use of the menstrual cup compared to their usual strategy for fistula management. This question uses likert-type responses to note whether the respondent perceives their urine leakage markedly improved, slightly improved, no change, slightly worse, or markedly worse.

Sponsors and collaborators

Lead sponsor

University of Ghana Medical School

Other

Collaborators

  • Korle-Bu Teaching Hospital, Accra, Ghana
  • NYU Langone Health
  • New York University

Registry information

Official study title

Feasibility of the Menstrual Cup for Non-Surgical Management of VVF Among Women Seeking Care at a Health Facility in Ghana

Acronym: FMCVVF

Important dates

Study start
2016
Primary completion
2016
Study completion
2016
First posted
Jan 29, 2018
Registry last updated
May 5, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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