Study in Women With Idiopathic Menorrhagia to Determine the Reduction in Menstrual Blood Loss (MBL) After Treatment With the Levonorgestrel-releasing Intrauterine System (IUS)

Completed · Phase 3

Conditions studied: Menorrhagia

In brief

The purpose of this study is to determine whether the levonorgestrel-releasing intrauterine system is effective in decreasing menstrual blood loss.

Key facts

Study ID

NCT00360490

Run by

Bayer

People needed

165

Starts

2006-07-01

Expected to finish

2008-06-01

Last updated by the study team

2013-12-09

Who can join

Age: 18 and older. Sex: female. Healthy volunteers: not accepted.

You may qualify if…

• Women who have >/= 80 mL blood loss during their menstrual cycles and desire contraception

You may not qualify if…

• Post menopausal menstrual cycle < 21 days or > 35 days
• Pregnancy

Where it is running

• Study site — Beverly Hills, California, United States
• Study site — Carmichael, California, United States
• Study site — San Diego, California, United States
• Study site — San Diego, California, United States
• Study site — Santa Monica, California, United States
• Study site — Torrance, California, United States
• Study site — Littleton, Colorado, United States
• Study site — Boynton Beach, Florida, United States
• Study site — Jacksonville, Florida, United States
• Study site — West Palm Beach, Florida, United States
• Study site — Boise, Idaho, United States
• Study site — Chicago, Illinois, United States
• Study site — Newburgh, Indiana, United States
• Study site — South Bend, Indiana, United States
• Study site — Amite, Louisiana, United States
• Study site — Marrero, Louisiana, United States
• Study site — Boston, Massachusetts, United States
• Study site — Saginaw, Michigan, United States
• Study site — Chesterfield, Missouri, United States
• Study site — Lincoln, Nebraska, United States
• Study site — Las Vegas, Nevada, United States
• Study site — LasVegas, Nevada, United States
• Study site — Moorestown, New Jersey, United States
• Study site — New Brunswick, New Jersey, United States
• Study site — Tucson, Arizona, United States

Full record on ClinicalTrials.gov

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