ClinicalTrials.Veeva

Menu

Validation of the Adenomyosis Calculator

University of Oslo (UIO) logo

University of Oslo (UIO)

Status

Completed

Conditions

Adenomyosis
Pelvic Pain Syndrome

Study type

Observational

Funder types

Other

Identifiers

NCT04135118
OUS P360

Details and patient eligibility

About

Adenomyosis is a disease where ectopic endometrial glands affect the muscular wall of the uterus. Women that suffer from dysmenorrhea or infertility caused by adenomyosis need to confirm or rule out adenomyosis, and therefore tools for non-histologic confirmation of adenomyosis are indubitably required. Transvaginal ultrasound has been shown to be useful in diagnosing adenomyosis, but the interpretation of findings requires significant expertise in ultrasound and experience with diagnosing adenomyosis. This is because adenomyosis shows a very heterogeneous appearance in ultrasound. There are many different diagnostic signs that have to be considered and weighed.

In a previous study, the investigators have developed a diagnostic algorithm that helps clinicians diagnose adenomyosis with transvaginal ultrasound and a clinical examination. It showed good diagnostic accuracy and seemed to be very robust with regards to artifacts and experience of the examiner. It is now necessary to validate this prediction model in a new, prospective study so it can be used in clinical practice.

Enrollment

500 patients

Sex

Female

Ages

Under 52 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Premenopausal (defined by having had menstruation the last six month)
  • If amenorrhea with levonorgestrel intrauterine device, the woman should be < 45 years old
  • Hysterectomy planned due to a benign condition
  • Hysterectomy does not require morcellation it is allowed to divide the uterus into 2-3 pieces, given that the orientation of the specimen is still possible for the pathologist)
  • Written consent is given
  • Can communicate in Norwegian or English at the Norwegian study sites, and Finnish, Swedish or English at the Finnish study site.

Exclusion criteria

  • Gynecological cancer present at the time of inclusion
  • Use of gonadotropin-releasing hormone agonist or antagonist within the last 3 months prior to the ultrasound evaluation
  • Prior endometrial ablation or resection
  • Postmenopausal status or no menstrual bleeding for the last 6 months, or amenorrhea with levonorgestrel-intrauterine device and age >45 years.
  • Need for morcellation of the uterus

Trial contacts and locations

5

Loading...

Central trial contact

Tina Tellum, MD

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems