Status:

COMPLETED

A Study to Gather Information About User Satisfaction in Women in Russia Who Take Estradiol Valerate/Dienogest

Lead Sponsor:

Bayer

Conditions:

Oral Contraception

Eligibility:

FEMALE

18-35 years

Brief Summary

Researchers want to learn more about user satisfaction in women in Russia who take estradiol valerate/ dienogest as a contraceptive in real conditions. Estradiol valerate/ dienogest is a form of birt...

Eligibility Criteria

Inclusion

  • Inclusion Criteria:
  • Age from 18 to 35 y.o.
  • Indications for administration of estradiol valerate/ dienogest for the purpose of oral contraception.
  • Patients who did not take estradiol valerate/ dienogest for at least one month before enrollment into the study.
  • Signed informed consent to participate in the study
  • Exclusion criteria
  • Participation in an investigational program with interventions outside of routine clinical practice.
  • Contraindications to estradiol valerate/ dienogest according to the local market authorization.
  • Any medical and non-medical reasons that according to the physician's judgment may prevent patient's participation in the non-interventional study.

Exclusion

    Key Trial Info

    Start Date :

    June 24 2021

    Trial Type :

    OBSERVATIONAL

    Allocation :

    ACTUAL

    End Date :

    April 20 2023

    Estimated Enrollment :

    255 Patients enrolled

    Trial Details

    Trial ID

    NCT04901377

    Start Date

    June 24 2021

    End Date

    April 20 2023

    Last Update

    September 18 2023

    Active Locations (1)

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    Many locations

    Multiple Locations, Russia