Actively Recruiting

Age: 35Years - 50Years
FEMALE
NCT07406412

Hormonal Regulation of Cardiometabolic Health Study

Led by University of Jyvaskyla · Updated on 2026-05-06

120

Participants Needed

7

Research Sites

148 weeks

Total Duration

On this page

Sponsors

U

University of Jyvaskyla

Lead Sponsor

W

Wellbeing Services County of Central Finland

Collaborating Sponsor

AI-Summary

What this Trial Is About

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 volunteer adipose tissue samples collected during surgery.

CONDITIONS

Official Title

Hormonal Regulation of Cardiometabolic Health Study

Who Can Participate

Age: 35Years - 50Years
FEMALE

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 35-50 years
  • Pre- or perimenopausal status defined by self-reported menstrual bleeding and/or follicle-stimulating hormone ≤25 IU/L
  • Having one or two functional ovaries
  • Planning to undergo bilateral or unilateral oophorectomy or salpingo-oophorectomy for non-malignant reasons
Not Eligible

You will not qualify if you...

  • Oophorectomy due to ovarian cancer or other malignant conditions
  • Current use of systemic estrogen-containing medication
  • Severe heart or liver disease preventing participation in physiological assessments
  • Mobility limitations that prevent participation in physical exercise tests

AI-Screening

AI-Powered Screening

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Trial Site Locations

Total: 7 locations

1

HUS

Helsinki, Finland, 00290

Not Yet Recruiting

2

University of Jyväskylä

Jyväskylä, Finland, 40014

Active, Not Recruiting

3

Wellbeing Services County of Central Finland

Jyväskylä, Finland, 70210

Actively Recruiting

4

Wellbeing Services County of North Savo

Kuopio, Finland, 70210

Actively Recruiting

5

Wellbeing Services County of North Ostrobothnia

Oulu, Finland, 90029

Not Yet Recruiting

6

Wellbeing Services County of Pirkanmaa

Tampere, Finland, 33520

Actively Recruiting

7

Wellbeing Services County of Southwest Finland

Turku, Finland, 20520

Actively Recruiting

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Research Team

E

Eija K Laakkonen, Associate Professor

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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