Clinical trial

Study in Women With Idiopathic Menorrhagia to Determine the Reduction in…

NCT00360490 · Bayer, Industry · Completed

Key facts

NCT number NCT00360490
Title Study in Women With Idiopathic Menorrhagia to Determine the Reduction in Menstrual Blood Loss (MBL) After Treatment With the Levonorgestrel-releasing Intrauterine System (IUS)
Official title A Multicenter, Randomized, Open Label, Parallel Group, Active Control Study to Evaluate the Efficacy and Safety of LNG IUS (Mirena®) as Compared to Medroxyprogesterone Acetate During 6 Cycles of Treatment in Patients With Idiopathic Menorrhagia
Lead sponsor Bayer, Industry
Status Completed
Phase Phase 3
Study type Interventional
Conditions Menorrhagia
Intervention type Drug
Interventions Levonorgestrel IUS (Mirena, BAY86-5028), Medroxyprogesterone acetate
Enrollment 165
Start date Jul 1, 2006
Primary completion Jun 1, 2008
Completion Jun 1, 2008
First posted Aug 4, 2006
Last update posted Dec 9, 2013
Countries Argentina, Brazil, Canada, Mexico, United States

At a glance

  • Yes Results posted
  • None Linked FDA submissions

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About ClinicalTrials.gov studies

ClinicalTrials.gov is the U.S. National Library of Medicine's registry of clinical studies conducted around the world. Contact and investigator details are not shown here.

Source: U.S. National Library of Medicine (NLM), ClinicalTrials.gov · Source date:

Browse all ClinicalTrials.gov studies