A pilot study to investigate the role of androgens in the sexual functioning of women with primary ovary insufficiency (POI).

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

NL-OMON

Registry ID

NL-OMON28298

Enrollment

Registered

2010-11-04

Start date

2010-11-26

Completion date

Unknown

Last updated

2024-02-28

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

Conditions

POI, POF, sexual dysfunction

Interventions

None listed

Eligibility

Inclusion criteria

Inclusion criteria: 1. Participating in the POI-trial in Utrecht; 2. Being treated for POI at the AMC, Amsterdam.

Exclusion criteria

Exclusion criteria: 1. Oophorectomy; 2. Severe relationship problems.

Design outcomes

Primary

Measure	Time frame
Hormone levels: 1. Estradiol; 2. Total testosterone; 3. Bio-available testosterone; 4. SHBG; 5. Androstenedione; 6. Dehydroepiandrosterone sulfate. Sexual function: 1. Genital response by VPA; 2. Subjective response by questionnaires, FSFI & FSDS-R. Implicit association tasks: 1. stIAT; 2. PAT; 3. Dot detection task.	—

Secondary

Measure	Time frame
The feasibility of these tests in this group, measured by interview.	—

Contacts

Public ContactSarah Coppes

AMC, Department of Sexology and Psychosomatic Obstetrics and Gynaecology, H4-205

sarah.coppes@student.uva.nl

Outcome results