Menopausal Impact of Opportunistic Salpingectomy for Ovarian Cancer Prevention
- Sponsor
- Umeå University
- Study ID
- NCT07423143
- Status
- Not Yet Recruiting
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Conditions
- Menopause
- Opportunistic Salpingectomy
Eligibility Criteria
- Sex
- FEMALE
- Age
- 20 Years - 65 Years
- Healthy Volunteers
- Not accepted
Interventions
- Opportunistic salpingectomy — PROCEDURERemoval of the fallopian tubes at the time of hysterectomy
Study Details
The goal of this clinical trial is to find out whether removing the fallopian tubes at the time of hysterectomy leads to an earlier menopause. The study includes women under 55 years of age who previously underwent hysterectomy as participants in the HOPPSA trial, where they were randomly assigned to either removal of the fallopian tubes or no removal. The main question is: • Does removing the fallopian tubes at the time of hysterectomy lead to an earlier menopause? Researchers will compare women who had their fallopian tubes removed during hysterectomy with women who had hysterectomy alone to see whether menopause occurs earlier after tube removal. Age at menopause will be estimated by measuring follicle-stimulating hormone (FSH) in small blood samples collected on a paper card. Participants will: * Collect 4-5 drops of blood using a finger prick * Place the drops on a paper card and mail it to the researchers * Complete an online questionnaire These steps will be done twice, one year apart.
Key Dates
- First listed
- Feb 20, 2026
- Start date
- Mar 31, 2026
- Status verified
- Feb 2026
- Primary completion
- Feb 28, 2029
- Completion
- Dec 31, 2057
Study Design
- Enrollment
- 2,100 participants (estimated)
- Allocation
- RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- TREATMENT
Arms
- Experimental: Opportunistic salpingectomySalpingectomy at the time of hysterectomy for a benign reason
- No Intervention: No salpingectomyNo salpingectomy at hysterectomy for a benign reason
Primary Outcome Measure
Age at menopause [ Time Frame: 1 year ]
Central Contacts
- Annika Idahl, MD, PhD, Professor+46 90 786 73 18
- Camilla Ersviken, Trial coordinator
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