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

Hopital Foch

Status: Completed

Conditions: Sexuality; Delivery

Treatments: Other: Survey

Study type: Observational

Funder types: Other

Identifiers

NCT03953573

2018_0057

Details and patient eligibility

About

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.

Enrollment: 105 patients

Sex: Female

Ages: 18 to 45 years old

Volunteers: Accepts Healthy Volunteers

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

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

Trial design

105 participants in 1 patient group

Women post-delivery

Treatment:

Other: Survey