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Clinical Trials in Norway / NCT04791033
Active, not recruiting Observational

Quality of Life After Hysterectomy (AdenoQOL)

NCT04791033 · tracked via the Priya Life Science Norway tracker
Phase
Observational
Started
2021-03-18
Last updated
2024-04-19

Condition(s) studied

AdenomyosisQuality of Life

Investigational drug(s) / intervention(s)

Hysterectomy

Hysterectomy: Elective procedure with hysterectomy due to benign gynecological condition

Study summary

Adenomyosis is a disease where ectopic endometrial-like glands affect the muscular wall of the uterus. About 70% of women affected by adenomyosis suffer from dysmenorrhea and menorrhagia. A levonorgestrel-releasing intrauterine device (LNG-IUD) is the first-choice treatment of adenomyosis, but is not always sufficiently effective in all women. Those women often end up removing the uterus (hysterectomy).

Hysterectomy is clinically regarded to be an efficient and final treatment of adenomyosis, but pelvic pain may also prevail after removal of the uterus. This study aimes to investigate the short - and long-term impact of hysterectomy on quality of life (QOL) and sexual function in women with adenomyosis, and further to evaluate if there is any difference compared to women that are removing their uterus due to other benign gynecological conditions.

Eligibility

Sex
FEMALE
Min age
18 Years
Max age
52 Years
Healthy volunteers
No
Inclusion Criteria: * Premenopausal status defined by having had menstruation within the last 12 months, or age \< 50 years if amenorrhea due to hormonal treatment * Hysterectomy planned due to a benign condition * Able to communicate in Norwegian or English * Electronic consent given Exclusion Criteria: * Age \< 18 years, postmenopausal status or no menstrual bleeding for the last 12 months * Hysterectomy as part of female-to-male transition * Pelvic organ prolapse as an indication for hysterectomy * Gynecological cancer suspected at the time of inclusion * Not able to communicate in Norwegian or English

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Marianne Omtvedt Oslo Norway

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT04791033 on ClinicalTrials.gov ↗ ← All trials in Norway