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Sexual function in women with prior severe preeclampsia.

Sexual function in women with prior severe preeclampsia. - S-FUPEC

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON56651
Enrollment
122
Registered
2024-03-14
Start date
2024-03-26
Completion date
Unknown
Last updated
2024-04-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

hypertension in pregnancy Preeclampsia

Interventions

None listed

Sponsors

Erasmus MC, Universitair Medisch Centrum Rotterdam
Lead Sponsor

Eligibility

Age
18 Years to 64 Years

Inclusion criteria

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

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.

Design outcomes

Primary

MeasureTime frame
General sexual function, as measured with the Female Sexual Function Index (FSFI) and sexual distress as measured with the Female Sexual Distress Scale-Revised (FSDS-R).

Secondary

MeasureTime frame
Sexual dysfunction, defined as a FSFI lower than 26.55 and FSDS-R >=15.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)