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Pelvic Floor Function After Vaginal and Cesarean Delivery Among Egyptian Women

Cairo University (CU) logo

Cairo University (CU)

Status

Unknown

Conditions

Pelvic Floor Disorders

Treatments

Diagnostic Test: female sexual function index

Study type

Observational

Funder types

Other

Identifiers

Details and patient eligibility

About

A cross sectional study for assessment of pelvic floor functions after 6 months to 4 years after normal vaginal delivery or Cesarean section

Full description

A cross sectional study for assessment of pelvic floor functions after 6 months to 4 years after normal vaginal delivery or Cesarean section Four separate entities were evaluated using internationally recognized and validated questionnaires:

  1. Pelvic organ prolapse evaluated using the Pelvic Organ Prolapse Distress Inventory
  2. Urinary functions were evaluated using the International Consultation on Incontinence Questionnaire Short Form
  3. Fecal incontinence was evaluated using Wexner Fecal Incontinence Score
  4. Sexual functions were evaluated using female sexual function index

Enrollment

5,000 estimated patients

Sex

Female

Ages

18 to 40 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • primiparity,
  • singleton pregnancy
  • cephalic presentation
  • term delivery (38-42 weeks).

Exclusion criteria

  • Women with operative vaginal delivery (vacuum extraction or forceps delivery)
  • women who had another delivery between the time of first one and time of evaluation
  • women with neurological diseases
  • women with vascular diseases and Diabetes Mellitus

Trial design

5,000 participants in 2 patient groups

vaginal delivery
Description:
Women underwent non complicated non instumental normal vaginal delivery
Treatment:
Diagnostic Test: female sexual function index
Cesarean section
Description:
Women underwent elective Cesarean section
Treatment:
Diagnostic Test: female sexual function index

Trial contacts and locations

1

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Central trial contact

Ahmed Maged, MD

Data sourced from clinicaltrials.gov

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