Eligibility Module

Eligibility Module

The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.

Eligibility Module path is as follows:

Study -> Protocol Section -> Eligibility Module

Eligibility Module


Ignite Creation Date: 2025-12-25 @ 5:03 AM
Ignite Modification Date: 2025-12-25 @ 5:03 AM
NCT ID: NCT04135118
Eligibility Criteria: 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
Healthy Volunteers: False
Sex: FEMALE
Maximum Age: 52 Years
Study: NCT04135118
Study Brief:
Protocol Section: NCT04135118