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OpenTrials
Completed

NCT Number: NCT00883662

Mirena Observational Program

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

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Key information

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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.

Treatment and study plan

Levonorgestrel (Mirena, BAY86-5028)

Drug

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

Primary outcomes

  1. Patient distribution per indication

    Time frame: 12 months

Secondary outcomes

  1. Patient compliance

    Time frame: 12 months

Sponsors and collaborators

Lead sponsor

Bayer

Industry

Registry information

Important dates

Study start
2009
Primary completion
2014
Study completion
2015
First posted
Apr 20, 2009
Registry last updated
Sep 30, 2016

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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