Non-interventional Study of Long-term Intrauterine Contraceptives Acceptability and User Satisfaction

• Status: Completed
• Trial end date: 2014-10-01
• Target enrollment: 0
• Participant gender: Female

Summary

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).

• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: Bayer
• Treatments: Contraceptive Agents; Copper; Levonorgestrel

Criteria

Inclusion Criteria:

• Women 20-40 years old

• Parity ≥ 1 child

• Requesting long-term contraception

• Written informed consent.

Exclusion Criteria:

• in accordance with the current leaflet