This is local prospective, non-interventional multi-center comparative study. Primary study objective is evaluation of the user satisfaction with Mirena or Copper IUD up to 1 year after insertion ( patient assessment questionnaire) in daily practice. For each patient, the treating gynecologist documents demographics, medical data, safety parameters and treatment signs and symptoms at an initial visit and one or two follow-up visit(s).
Study Type
OBSERVATIONAL
Enrollment
2,348
intrauterine system containing 52 mg levonorgestrel, with daily release of 20 mcg levonorgestrel
Copper device, inserted intrauterine
Unnamed facility
Many Locations, Russia
User satisfaction of the contraception method with Mirena or Copper IUD
Time frame: up to 12 months
Safety evaluation of Mirena or Copper IUD in routine practice Safety parameters include number of AEs, severity,relationship to Mirena or Cooper IUD
Time frame: up to 12 months
Contraceptive reliability of Mirena or Cooper IUD in routine practice ( fixing number of pregnancies)
Time frame: up to 12 months
Continuation/discontinuation rate ( number of cases with contraceptive method continuation and discontinuations)
Time frame: up to 12 months
Relationship between different parameters and women preferences in choosing Mirena or Cooper IUD as their contraceptive method ( demographic parameters, age group, residence, reproductive history and plans, etc.) using patients questionnaire
Time frame: up to 12 months
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