Hopital Foch
Suresnes, France
NCT Number: NCT03953573
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.
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Notify Me18 year–45 year
Female
Observational
Suresnes, France
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Survey completed at 1 day, 8 days 1 or 3 months post delivery
Time frame: 3 months
Time to sexuality resumption
Time frame: 1 month
Number of women receiving advice from a health professional
Time frame: 3 months
Number of women needed pain treatment or with problem for sexuality resumption
Time frame: 3 months
Frequency of sex
Hopital Foch
Other
Acronym: SMD
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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