Overview

Trial Comparing Preoperative Dienogest Therapy Followed by Surgery vs. Upfront Surgery to Save Ovarian Reserve in Young Women With Ovarian Endometrioma

Status:
Withdrawn
Trial end date:
2018-03-01
Target enrollment:
0
Participant gender:
Female
Summary
Randomized phase 2 trial comparing preoperative dienogest therapy followed by surgery vs. upfront surgery to save ovarian reserve in young women with ovarian endometrioma
Phase:
Phase 2
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Seoul National University Hospital
Collaborators:
Ajou University School of Medicine
Asan Medical Center
Ewha Womans University Mokdong Hospital
Korea University Guro Hospital
Kyung Hee University Hospital at Gangdong
Treatments:
Dienogest
Nandrolone
Criteria
Inclusion Criteria:

- Unilateral ovarian endometrioma ≥ 5cm or bilateral ovarian endometriomas with any size
diagnosed by ultrasonography.

- In Patients with previous unilateral salpingo-oophorectomy (USO)

- Unilateral ovarian endometrioma with any size is eligible

- 20 ≤ Age ≤ 45 and premenopause

- Plan to undergo conservative surgery for endometriomas

Exclusion Criteria:

- Pregnant women or women who were suspected to be pregnant

- Women with current venous thromboembolism or history of such diseases

- Women with current arterial disease or cardiovascular diseases (e.g. myocardial
infarction, cerebrovascular diseases, or ischemic heart diseases) or history of such
diseases

- Women with current diabetes with vascular lesions or history of such diseases

- Women with current severe liver diseases or history of severe liver diseases with
abnormal liver function

- Women with current liver tumor or history of liver tumor

- Women with current or history of sex-hormone dependent malignant tumor or women who
were suspected to have a sex-hormone dependent malignant tumor

- Women with vaginal bleeding of unknown causes

- Women with a history of allergic reaction to elements of DNG

- Women with galactose intolerance, Lapp lactase deficiency, glucose-galactose
malabsorption

- Women whose non-compliance is expected

- Lactation (treatment with DNG is not recommended in lactating women due to possible
excretion in breast milk)

- Any medication that could result in an excessive accumulation, impaired metabolism, or
altered excretion of the study drug or might interfere with the conduct of the study
or the interpretation of the results