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

NCT03953573 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 105

Last updated 2021-03-16

No results posted yet for this study

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.

Conditions

  • Sexuality
  • Delivery

Interventions

OTHER

Survey

Survey completed at 1 day, 8 days 1 or 3 months post delivery

Sponsors & Collaborators

  • Hopital Foch

    lead OTHER

Eligibility

Min Age
18 Years
Max Age
45 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2018-12-22
Primary Completion
2020-12-08
Completion
2020-12-08

Countries

  • France

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03953573 on ClinicalTrials.gov