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Effects of Pregnancy and Childbirth on Pelvic Floor Morphology and Sexual Function in Egyptian Women

Effects of Pregnancy and Parturition on Pelvic Floor Morphology and Sexual Function in Egyptian Women.

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02245386
Enrollment
120
Registered
2014-09-19
Start date
2013-05-31
Completion date
2014-04-30
Last updated
2014-09-19

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

Conditions

Pregnancy, Childbirth and Puerperal Disorders

Brief summary

To evaluate levator ani muscle morphology following normal vaginal delivery and cesarean section (elective and emergent), using three-dimensional (3D) transperineal ultrasound, and to study the effect of mode of delivery on female sexual function.

Detailed description

1. transperineal pelvic floor ultrasound applied for the submitted 120 women primiparae (40 women after normal vaginal delivery), (40 women after urgent cesarean section), (40 women after elective cesarean section), in early postpartum period (48 to 72) hours postpartum, to evaluate levator ani morphology. 2. answering of the validated female sexual function index (F.S.F.I) three months postpartum period for same cases submitted to ultrasound.

Interventions

RADIATIONtransperineal pelvic floor ultrasound

Transperineal pelvic floor ultrasound applied for the submitted 120 women primiparae (40 women after normal vaginal delivery), (40 women after urgent cesarean section), (40 women after elective cesarean section), in early postpartum period (48 to 72) hours postpartum, to evaluate levator ani morphology.

Sponsors

Al-Azhar University
Lead SponsorOTHER

Study design

Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
FEMALE
Healthy volunteers
No

Inclusion criteria

* primiparae in early postpartum period (48 hours to72 hours). written consent was taken. easy communicable, reachable women for further requirements.

Exclusion criteria

1. Refused consent. 2. Previous vaginal or cesarean delivery. 3. Severe mental illness. 4. Severe physical handicap or difficulties in communication. 5. Women without postpartum active sexual life or separate from their spouse. 6. Past history of sexual dysfunction.

Design outcomes

Primary

MeasureTime frame
Pelvic floor muscle strength as assessed by three/four dimensional translabial pelvic floor ultrasoundearly postpartum period (48 to 72) hours postpartum
Sexual function of pelvic floor as assessed by the validated female sexual function indexat 3 months after delivery

Secondary

MeasureTime frame
Trauma or avulsion of levator ani muscle as assessed by three/four dimensional translabial pelvic floor ultrasound6 months after delivery.
Sexual function as assessed by the validated female sexual function index3 months after delivery

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026