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:
2025-12-24 @ 5:30 PM
Ignite Modification Date:
2025-12-24 @ 5:30 PM
NCT ID:
NCT03509168
Eligibility Criteria:
Inclusion Criteria:
* Reproductive age (15-49 years)
* Documented symptomatic uterine fibroids by ultrasound imaging
* Presenting to any of the selected hospitals within the study period.
* Scheduled for open myomectomy
* Willing to give informed consent
Exclusion Criteria:
* Previous uterine surgeries.
* Poorly controlled hypertension or diabetes
* History of a bleeding disorder, concurrent anticoagulant therapy, family history of bleeding disorder, prior history of deep venous thrombosis.
* Pregnancy
* Hemoglobin less than 10.5 g/dL at the time of surgery
* Prior treatment using GnRH analogues
* Intra-operative exclusion; pelvic endometriosis, adenomyosis, pelvic abcesses, pelvic malignancies
Healthy Volunteers:
False
Sex:
FEMALE
Minimum Age:
15 Years
Maximum Age:
49 Years
Study:
NCT03509168
Study Brief:
Protocol Section:
NCT03509168