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CompletedNCT01753258

Outcomes of Delivery in Patients With Dyspareunia

Outcomes of Delivery in Patients With Dyspareunia- A Prospective Study

Status
Completed
Phase
Study type
Observational
Enrollment
173 (actual)
Sponsor
Hadassah Medical Organization · Academic / Other
Sex
Female
Age
18 Years – 50 Years
Healthy volunteers
Accepted

Summary

The focus of this pilot study is to determine if a woman who experiences pain during sexual intercourse has a higher risk of complications during labor and delivery secondary to pelvic floor dysfunction, anxiety and intolerance towards pelvic examinations. Furthermore, it is unclear whether women with prepartum dyspareunia experience an improvement following vaginal delivery. While physicians may expect that vaginal birth improves dyspareunia due to the stretching effect on pelvic floor, to date, there is insufficient evidence to support this claim. The Investigators plan to prospectively study 200 patients at our Institution, collect information regarding birth and follow them, via questionnaires, regarding their dyspareunia postpartum.

Conditions

Timeline

Start date
2013-01-01
Primary completion
2016-09-01
Completion
2016-09-01
First posted
2012-12-20
Last updated
2016-10-11

Locations

1 site across 1 country: Israel

Source: ClinicalTrials.gov record NCT01753258. Inclusion in this directory is not an endorsement.

Outcomes of Delivery in Patients With Dyspareunia (NCT01753258) · Clinical Trials Directory