← Eichor
Study identifier: NCT07406412 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Hormonal Regulation of Cardiometabolic Health Study

Condition: Menopause Surgical  ·  Sponsor: University of Jyvaskyla

PhaseN/A
Planned participants120
Who can joinFemale, 35 Years to 50 Years
Healthy volunteersNo

About this study

The goal of this observational study is to understand how the loss of ovarian function after oophorectomy affects the health and well being of women aged 35-50. The study focuses on four areas: 1. Quality of life and embodied experience, 2. Cardiometabolic health, 3. Central nervous system function, and 4. Adipose tissue health and cellular function. Our primary goal is to understand the effects of oophorectomy on women's health in focus areas 1 to 3. To do this, we will compare women's health before surgery with follow up assessments at 1-2 months and 12 months after surgery. Some participants may start hormone replacement therapy (HRT) during follow up as part of their routine care; this is outside the study protocol. As an exploratory aim, we will examine whether 12 month outcomes-or the change from baseline to 12 months-differ between participants who begin HRT and those who do not. Focus area 4 provides an opportunity to explore how molecular and cellular mechanisms in adipose tissue respond to the loss of ovarian hormones. These analyses are exploratory and intended to offer mechanistic insight rather than clinical endpoints. Participants will: * undergo bilateral (or unilateral, if only one ovary remains) oophorectomy as part of their clinical treatment, * complete questionnaires and physiological measurements at three time points, * a subgroup will participate in qualitative interviews about their lived experience of surgical menopause, * and a subgroup will vol…

This description comes directly from the study's public registry record.

Talk to the study team

Eija K Laakkonen, Associate Professor  ·  +358-40-8053588  ·  eija.k.laakkonen@jyu.fi

Always discuss trial participation with your own doctor first.

Locations (7)

HUSHelsinki, FinlandNot Yet Recruiting
University of JyväskyläJyväskylä, FinlandActive Not Recruiting
Wellbeing Services County of Central FinlandJyväskylä, FinlandRecruiting
Wellbeing Services County of North SavoKuopio, FinlandRecruiting
Wellbeing Services County of North OstrobothniaOulu, FinlandNot Yet Recruiting
Wellbeing Services County of PirkanmaaTampere, FinlandRecruiting
Wellbeing Services County of Southwest FinlandTurku, FinlandRecruiting

Follow this study

Get one email when the public record changes — results posted, or the study's status changes. Nothing else, ever.

We email about this public record only. Unsubscribe anytime with one click. Never medical advice.

Is this your study? This page was generated automatically from the public registry record. Sponsors can claim it — free — to add branding and verified contact routing. Claim this page →

This page is independently generated by Eichor from the public ClinicalTrials.gov record and re-synced daily. It is not the sponsor's official website unless claimed. Nothing here is medical advice; eligibility is always determined by the study team — talk to your own doctor first.

Source record: clinicaltrials.gov/study/NCT07406412