Pain Associated With Endometriosis

Completed · Phase 2 · Has a placebo group

Conditions studied: Endometriosis

In brief

This study will evaluate the efficacy and safety of an investigational medication compared with placebo in the treatment of pain associated with endometriosis.

Key facts

Study ID

NCT00758953

Run by

Lumara Health, Inc.

People needed

66

Starts

2007-02-01

Expected to finish

2009-01-01

Last updated by the study team

2012-03-06

Who can join

Age: 18 and older, up to 50. Sex: female. Healthy volunteers: not accepted.

You may qualify if…

• Menstruating female 18-50 years of age,
• Regular cycle length of 21 to 35 days with menstrual bleeding that typically lasts no more than 7 days,
• Has pain associated with endometriosis,
• Has a documented history consistent with endometriosis,

You may not qualify if…

• Is pregnant or lactating,
• Has a history of or has active thrombosis

Where it is running

• Study site — Chandler, Arizona, United States
• Study site — Phoenix, Arizona, United States
• Study site — Phoenix, Arizona, United States
• Study site — Little Rock, Arkansas, United States
• Study site — Carmichael, California, United States
• Study site — San Diego, California, United States
• Study site — San Diego, California, United States
• Study site — San Diego, California, United States
• Study site — Denver, Colorado, United States
• Study site — Britain, Connecticut, United States
• Study site — West Hartford, Connecticut, United States
• Study site — Aventura, Florida, United States
• Study site — Boynton Beach, Florida, United States
• Study site — Clearwater, Florida, United States
• Study site — Hudson, Florida, United States
• Study site — Tampa, Florida, United States
• Study site — Alpharetta, Georgia, United States
• Study site — Atlanta, Georgia, United States
• Study site — Decatur, Georgia, United States
• Study site — Boise, Idaho, United States
• Study site — Boise, Idaho, United States
• Study site — Champaign, Illinois, United States
• Study site — Baton Rouge, Louisiana, United States
• Study site — Chesterfield, Missouri, United States
• Study site — Moorestown, New Jersey, United States

Full record on ClinicalTrials.gov

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