Phase
Condition
Chronic Pain
Endometriosis
Pain
Treatment
Placebo - Cap
Cabergoline 0.5 MG
Clinical Study ID
Ages 15-40 Female
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
Female with surgically-confirmed endometriosis
Age 15 years to 40 years
Current use ≥ 2 months duration of hormonal therapy such as combined oralcontraceptives, norethindrone acetate, or levonorgestrel intrauterine device
Current pelvic pain (score ≥ 3 on Visual Analog Scale, where 0 represents absence ofpain and 10 indicates unbearable pain) present for ≥ 14 days/month over the 2 monthsprior to study enrollment
Willingness to comply with visit schedule and protocol
Exclusion
Exclusion Criteria:
Pre-menarche or post-menopause
Contraindications to cabergoline (e.g., cardiac valve disorder; pulmonary,pericardial, retroperitoneal fibrotic disorder; hypersensitivity to ergotderivatives; uncontrolled hypertension)
Significant mental or chronic systemic illness that might confound pain assessmentor the ability to complete the study
Pregnant, breastfeeding, or planning to become pregnant in the next 6 months
Impaired liver function (ALT > 2x normal) or liver disease
Breast cancer, current or previous
Thromboembolic disease, current or previous
Use of other drugs that affect dopamine (e.g., phenothiazines, metoclopramide,butyrophenones)
Study Design
Study Description
Connect with a study center
Standford University
Palo Alto, California 94305
United StatesActive - Recruiting
Childrens Hospital Colorado
Aurora, Colorado 80045
United StatesActive - Recruiting
Beth Israel Deaconess Medical Center
Boston, Massachusetts 02115
United StatesActive - Recruiting
Brigham and Women's Hospital
Boston, Massachusetts 02115
United StatesActive - Recruiting
Children's Hospital Boston
Boston, Massachusetts 02115
United StatesActive - Recruiting
Thomas Jefferson University Hospital
Philadelphia, Pennsylvania 19107
United StatesActive - Recruiting
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