Status:

COMPLETED

Study to Evaluate the Effect of Six Cycles of Treatment With a Combined Oral Contraceptive (EE 0.30 mg/DRSP 3 mg) on Quality of Life.

Lead Sponsor:

Bayer

Conditions:

Healthy

Eligibility:

FEMALE

18-35 years

Phase:

PHASE3

Brief Summary

The purpose of this study is to evaluate the effects on the quality of life and BMI of new contraceptives.

Detailed Description

The study has previously been posted by Schering AG, Germany. Schering AG, Germany has been renamed to Bayer Schering Pharma AG, Germany.Bayer Schering Pharma AG, Germany is the sponsor of the trial.

Eligibility Criteria

Inclusion

  • Female requiring contraceptives.
  • Aged 18 to 35 if a non-smoker, aged 18 to 30 if a smoker.
  • Regular menstrual cycle (defined as duration of 28 +/- 5 days).

Exclusion

  • No Contraindication for OC use

Key Trial Info

Start Date :

December 1 2002

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

May 1 2004

Estimated Enrollment :

221 Patients enrolled

Trial Details

Trial ID

NCT00367276

Start Date

December 1 2002

End Date

May 1 2004

Last Update

October 11 2013

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