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Pelvic Floor Function Evaluation of Singleton Primiparae After Vaginal Delivery and Cesarean Section

NCT02661867 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 865

Last updated 2016-01-25

No results posted yet for this study

Summary

Objective of this longitudinal observational cohort study was to analyze incidence of pelvic floor dysfunction (PFD) symptoms, including pelvic organ prolapse (POP), urinary incontinence (UI), and fecal incontinence (FI), seven to twelve years after delivery, in two groups of singleton primiparae after vaginal delivery (VD) and cesarean section (CS).

Conditions

  • Pelvic Floor Disorders

Interventions

BEHAVIORAL

delivery

delivery either vaginal or by cesarean section

Sponsors & Collaborators

  • Brno University Hospital

    lead OTHER

Eligibility

Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2002-01-31
Primary Completion
2007-12-31
Completion
2014-12-31

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02661867 on ClinicalTrials.gov