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Mirena Observational Program


N/A
18 Years
N/A
Open (Enrolling)
Female
Contraception, Menorrhagia, Endometrial Hyperplasia, Estrogen Replacement Therapy

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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

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