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CompletedNCT03449355Updated Apr 3, 2018

Sexuality After Different Mode of Deliveris

An observational study in Sexual Dysfunction and the Mode of Deliveries, sponsored by Mansoura University. Completed at 1 site in Egypt. Open to female participants aged 20 Years to 30 Years. Per ClinicalTrials.gov, last updated 2018-04-03.

Sponsored by Mansoura University · Observational

Study type
Observational
Model
Other
Time perspective
Cross-sectional
Enrollment
100
Ages
20 Years to 30 Years
Sex
Female
01

Study summary

Pregnancy and delivery usually affect the general women's quality of life. Some studies have reported that sexual health may be affected by the mode of delivery. More than 70% of pregnant women prefer C-section due to several reasons point out the fear of pain and complications of vaginal delivery as the most common reasons.

Aim of the work: To explore the relationship between quality of life and the possible sexual dysfunction after normal vaginal in comparison to cesarean section deliveries.

02

Conditions studied

  • Sexual Dysfunction and the Mode of Deliveries

Keywords

  • sexuality
  • mode of delivery
  • quality of life
03

Who can participate

Ages eligible
20 Years to 30 Years
Sexes eligible
Female
Accepts healthy volunteers
No
Sampling method
Probability sample

Study population

primiparous women 6-12 months after deliveries either vaginal or cesarean section

Inclusion criteria

  • Primiparas women who had been delivered by either vaginal or cesarean section about 6-12months.
  • All included women should be officially married

Exclusion criteria

Exclusion Criteria:

  • Women with history of sexual dysfunction
  • Women with history of any pelvic surgery apart from Cesarean.
  • history of anti-depressive drug therapy.
  • history of genital prolapse
  • history of Diabetes mellitus
  • loss of any family member or unfaveorouble neonatal outcome or childdeath
  • Divorce experience
  • family problems and cases who were not interested in participation
04

Study design

Observational model
Other
Time perspective
Cross-sectional
Enrollment
100 participants (actual)
Patient registry
No

Groups and cohorts

  • vaginal group
  • cesarean section group
05

What researchers measure

Primary outcomes

  1. quality of life after delivery

    the amplitude of many changes occur during and after pregnancy, which affect physical, psychological and social health and generally women's quality of life

    Time frame: one month

Secondary outcomes

  1. the relationship between quality of life and sexual dysfunction after both modes delivery

    Time frame: one month

06

Study locations

1 site
  • Mansoura University
    Mansourah, 35516, Egypt
07

Registry details

Key details

Study ID
NCT03449355
Lead sponsor
Mansoura University
Responsible party
Hanan Nabil (Assistant professor, Mansoura University) — Principal investigator
First posted
Feb 28, 2018
Start date
Jan 11, 2018
Primary completion
Mar 1, 2018
Completion
Mar 1, 2018
Last update
Apr 3, 2018

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Mar 2018. You cannot join it, but the record below documents what was studied.

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