Oxytocin in Postmenopausal Women
Starting soon
Conditions studied: Postmenopausal, Premenopausal
In brief
The aim of the present study is to assess whether cumulative endogenous neurophysin I secretion over one month differs between premenopausal and postmenopausal women. Using repeated measurements of neurophysin-I (NP-I, equimolar surrogate marker of oxytocin) across defined physiological time points, this study investigates oxytocin system regulation under cyclic and non-cyclic hormonal conditions. The primary hypothesis is that cumulative NP-I release, expressed as the area under the curve (AUC) is lower in the postmenopausal group compared to the premenopausal group.
Key facts
- Study ID
- NCT07742124
- Run by
- University Hospital, Basel, Switzerland
- People needed
- 30
- Starts
- 2027-06-01
- Expected to finish
- 2027-09-01
- Last updated by the study team
- 2026-08-03
Who can join
Age: 18 and older. Sex: female. Healthy volunteers: not accepted.
You may qualify if…
- Female sex at birth
- Age ≥18 years
- Premenopausal group:
- Premenopausal women aged 18-35 years with regular menstrual cycles (21-35 days) for ≥3 months prior to study entry
- Postmenopausal group:
- Postmenopausal women ≥2 years of postmenopause (i.e. 3 years since last menstrual period (LMP), with menopause defined as ≥ 12 months of amenorrhea)
You may not qualify if…
- Pregnancy or breastfeeding
- Use of hormonal contraception or hormone replacement therapy within the last 3 months
- Known endocrine disorders affecting the hypothalamic-pituitary-gonadal axis
- Use of medications
- Severe depression (BDI score > 28 points), any other severe psychiatric illness or acute medical disease
- Inability to comply with study procedures
- Participation in a trial with investigational drugs within the last 30 days
Where it is running
- University Hospital Basel — Basel, Canton of Basel-City, Switzerland
Full record on ClinicalTrials.gov
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