Management of Post-delivery Pain and Its Impact on Resumption of Sexuality
NCT ID: NCT03953573
Last Updated: 2021-03-16
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
105 participants
OBSERVATIONAL
2018-12-22
2020-12-08
Brief Summary
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Survey to be completed by women at 8 and 15 days and 1 or 3 months after delivery.
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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Women post-delivery
Survey
Survey completed at 1 day, 8 days 1 or 3 months post delivery
Interventions
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Survey
Survey completed at 1 day, 8 days 1 or 3 months post delivery
Eligibility Criteria
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Inclusion Criteria
* 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
* BMI \> 30
* Conjugopathie
* Known psychiatric history
* Medical history with gynecologic impact
* Surgery history with gynecologic impacts
* Hysterectomy post-delivery
* Protected by French law
18 Years
45 Years
FEMALE
Yes
Sponsors
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Hopital Foch
OTHER
Responsible Party
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Locations
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Hopital Foch
Suresnes, , France
Countries
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Other Identifiers
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2018_0057
Identifier Type: -
Identifier Source: org_study_id
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