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Management of Post-delivery Pain and Its Impact on Resumption of Sexuality

Completed
Conditions
Sexuality
Delivery
Interventions
Other: Survey
Registration Number
NCT03953573
Lead Sponsor
Hopital Foch
Brief Summary

Study of management of pain and information given to women post-delivery and their impact of the resumption of sexuality.

Survey to be completed by women at 8 and 15 days and 1 or 3 months after delivery.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
Female
Target Recruitment
105
Inclusion Criteria
  • Primiparous woman
  • Age between 18 and 45 years old
  • Delivery after 37 weeks of amenorrhea
  • Speaking French
  • Pregnancy, delivery and new-born examination without morphologic or biometric abnormalities, respiratory distress and no pathology discovered at neonatal screening on day 3
  • Heterosexual woman with partner
  • Signed consent
  • Affiliate of national health insurance scheme
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Exclusion Criteria
  • Multiple pregnancy,
  • BMI > 30
  • Conjugopathie
  • Known psychiatric history
  • Medical history with gynecologic impact
  • Surgery history with gynecologic impacts
  • Hysterectomy post-delivery
  • Protected by French law
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Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Arm && Interventions
GroupInterventionDescription
Women post-deliverySurvey-
Primary Outcome Measures
NameTimeMethod
Post-delivery sexuality resumption3 months

Time to sexuality resumption

Secondary Outcome Measures
NameTimeMethod
Pain post-delivery3 months

Number of women needed pain treatment or with problem for sexuality resumption

Sexual health3 months

Frequency of sex

Discussion with healthcare professional on post-delivery sexuality1 month

Number of women receiving advice from a health professional

Trial Locations

Locations (1)

Hopital Foch

🇫🇷

Suresnes, France

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