Sexual function in women with prior severe preeclampsia.

• Conditions: 10010273; hypertension in pregnancy; Preeclampsia

• Registration Number: NL-OMON56651
• Lead Sponsor: Erasmus MC, Universitair Medisch Centrum Rotterdam

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 9 April 2024

Recruitment & Eligibility

• Status: Pending
• Sex: Not specified
• Target Recruitment: 122

Inclusion Criteria

- Being in between 9-15 months postpartum
- Aged above 18 years
- Being in a stable relationship for at least 6 months
- Diagnosis of severe preeclampsia, based on the ACOG definition or healthy
postpartum women without a history of severe preeclampsia.

Exclusion Criteria

- Pregnant women
- Having undergone a radical hysterectomy or prolapse surgery
- Usage of medications that are known to influence sexual response, with the
exception of contraceptive use.
- Medical disorders (other than a history of preeclampsia) that are known to
influence sexual response, such as heart failure or chronic obstructive
pulmonary disease.

Study & Design

• Study Type: Observational non invasive
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
<p>General sexual function, as measured with the Female Sexual Function Index<br /><br>(FSFI) and sexual distress as measured with the Female Sexual Distress<br /><br>Scale-Revised (FSDS-R).</p><br>

Secondary Outcome Measures

Name	Time	Method
<p>Sexual dysfunction, defined as a FSFI lower than 26.55 and FSDS-R >=15.</p><br>