Trial Information
Mirena Observational Program
Inclusion Criteria:
- Patients older than 18 years with previously taken decision of their gynecologist to
insert Mirena according to registered indications
Exclusion Criteria:
- All patients with contraindications to Mirena insertion, according to approved
prescribing information.
Type of Study:
Observational
Study Design:
Observational Model: Cohort, Time Perspective: Prospective
Outcome Measure:
Patient distribution per indication
Outcome Time Frame:
12 months
Safety Issue:
No
Principal Investigator
Bayer Study Director
Investigator Role:
Study Director
Investigator Affiliation:
Bayer
Authority:
Kazakhstan: National Center for Expertise of Medicinal Drugs
Study ID:
14474
NCT ID:
NCT00883662
Start Date:
June 2009
Completion Date:
July 2014
Related Keywords:
- Contraception
- Menorrhagia
- Endometrial Hyperplasia
- Estrogen Replacement Therapy
- Endometrial Hyperplasia
- Hyperplasia
- Menorrhagia
- Adenoma