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Mirena Observational Program

Mirena Observational Program

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT00883662
Enrollment
2725
Registered
2009-04-20
Start date
2009-05-31
Completion date
2015-11-30
Last updated
2016-09-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Contraception, Menorrhagia, Endometrial Hyperplasia, Estrogen Replacement Therapy

Brief summary

Mirena is used for long-term in Kazakhstan, and in our observational program we would like to study patients distribution per indications of Mirena, and also patient compliance within a year after Mirena insertion. For patients with all approved indications for Mirena use: contraception, treatment of menorrhagia and protection from endometrial hyperplasia during estrogen replacement therapy

Interventions

Patients older than 18 years with previously taken decision of their gynecologist to insert Mirena according to registered indications

Sponsors

Bayer
Lead SponsorINDUSTRY

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
No

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.

Design outcomes

Primary

MeasureTime frame
Patient distribution per indication12 months

Secondary

MeasureTime frame
Patient compliance12 months

Countries

Kazakhstan

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026