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Cohort studies for screening and treatment of pelvic floor dysfunction

Cohort studies for screening of postpartum pelvic floor function and treatment on postpartum pelvic floor dysfunction.

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1900021717
Enrollment
Unknown
Registered
2019-03-06
Start date
2019-04-01
Completion date
Unknown
Last updated
2019-03-11

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

Conditions

pelvic floor dysfunction

Interventions

intervention group:intra-vaginal eletrical stimulation
intervention group:pelvic muscle exercise
intervention group:Vaginal rehabilitator
control group:no invention

Sponsors

Beijing Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: Early postpartum during from 42 to 60 days, without history of pelvic organ prolapsed or urinary incontinence and absence of genital tract infection

Exclusion criteria

Exclusion criteria: delivery with more than third-degree laceration, history of mental disorders and without ability to sign informed consent

Design outcomes

Primary

MeasureTime frame
POP-Q;—

Secondary

MeasureTime frame
pelvic muscle strength;pelvic imaging measurement;related questionnaire;—

Countries

China

Contacts

Public ContactLi Min

Department of Gynecology and Obstetrics, Beijing Hospital National Center of Gerontology

mindy99999@126.com+86 13811526308

Outcome results

None listed

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