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Feasibility of the Menstrual Cup for VVF

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

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03414060
Acronym
FMCVVF
Enrollment
11
Registered
2018-01-29
Start date
2016-08-08
Completion date
2016-12-02
Last updated
2026-05-05

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Obstetric; Injury, Vaginal Fistula, Vesico Vaginal Fistula

Keywords

obstetric fistula, vesicovaginal fistula, menstrual cup, pad test, non-surgical management, feasibility, acceptability, innovation, coping, incontinence

Brief summary

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.

Detailed description

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.

Interventions

Sponsors

University of Ghana Medical School
Lead SponsorOTHER
New York University
CollaboratorOTHER
NYU Langone Health
CollaboratorOTHER
Korle-Bu Teaching Hospital, Accra, Ghana
CollaboratorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Intervention model description

repeated measures

Eligibility

Sex/Gender
FEMALE
Age
15 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1. Patient seeking surgical repair for VVF 2. VVF confirmed by gynecologic examination 3. Adequate vaginal capacity to accommodate the menstrual cup 4. Fistula high in vagina (determined at gynecologic examination) 5. Willingness to insert and remove the device by one's self

Exclusion criteria

1. Technically difficult to insert and or remove the menstrual cup (eg severely scarred vagina) 2. Unable or unwilling to learn to insert and remove the menstrual cup 3. Patient who declines consent or is incapable of consent 4. Presence of rectovaginal fistula (RVF) or combined RVF and VVF 5. Fistula low in the vagina precluding collection of urine by the menstrual cup

Design outcomes

Primary

MeasureTime frameDescription
Volume of urinary leakage (in ml)Over 2 hoursMeasured by 2-hr pad test

Secondary

MeasureTime frameDescription
Acceptability of the menstrual cupOver 2 hoursUsing 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.
Adverse eventsOver 2 hoursErythema, edema/induration, erosion, bleeding assessed by clinical exam
Rate of enrollment through study completionthrough study completion, an average of 1 yearNumber of individuals who enroll out of the total number of individuals screened
Rate of consent through study completionthrough study completion, an average of 1 yearNumber of individuals who complete the consent form out of the total number of screened individuals meeting all other inclusion and exclusion criteria
Perceived assessment of leakage with use of the menstrual cupAfter 1 hour of useProportion 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.

Countries

Ghana

Contacts

PRINCIPAL_INVESTIGATORGabriel YK Ganyaglo, MD

Korle-Bu Teaching Hospital, Accra, Ghana

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: May 6, 2026