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sexual dysfunction in incontinent women

A cross-sectional case control study of sexual dysfunction in incontinent women

Status
Active, not recruiting
Phases
Phase 4
Study type
Observational
Source
CTRI
Registry ID
CTRI/2020/02/023164
Enrollment
100
Registered
2020-02-06
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: N394- Other specified urinary incontinence

Interventions

Intervention1: Women with stress urinary incontinence: To determine the prevalence of Female Sexual Dysfunction (FSD) among Incontinent women presenting to the Urogynecology OPD in comparison to match

Sponsors

AIIMS Research Institute
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Incontinent women ready to talk about their sexual life and willing to fill in questionnaires relating sexual life and depression. 2. Recent sexual activity in the last 4 weeks

Exclusion criteria

Exclusion criteria: Pregnant women Vaginitis, PID , current UTI ï?· Sexually inactive women with no sexual activity in the past 4 weeks ï?· Women unwilling to talk about their sexual problems ï?· Sexually inactive women ï?· Previously failed Urinary Incontinence surgery ï?· Pelvic surgery or any Genital surgery ï?· Women with recent delivery in the past 6 weeks ï?· Women with S/S of PID ï?· Women with sexual dysfunction due to male partner issues ï?· Any congenital vaginal abnormalities ï?· Patients with neurological and mental illness ï?· Physical causes of depression ï?· Normal bereavement ï?· History of maniac/hypomaniac

Design outcomes

Primary

MeasureTime frame
to assess the prevalence of FSD in patients with Urinary Incontinence using validated questionnaires.Timepoint: after 3 months

Secondary

MeasureTime frame
NATimepoint: NA

Countries

India

Contacts

Public ContactDr Rajesh Kumari

All India Institute of Medical Sciences

drrajeshkumari@yahoo.com9911226176

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026