Assess Satisfaction of Patients and Physicians With Results of Yaz Plus Treatment for 13 Cycles

NCT02159261 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 1500

Last updated 2017-08-09

No results posted yet for this study

Summary

Local prospective multicenter non-comparative non-interventional observational study. It's planed to assess satisfaction of patients and physicians with results of Yaz Plus treatment for 13 cycles in real practice.

Conditions

  • Contraception

Interventions

DRUG

BAY98-7071_EE20/DRSP/L-5-MTHF

Patients treated by Physicians under approved local prescriptions

Sponsors & Collaborators

Principal Investigators

  • Bayer Study Director · Bayer

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2014-07-15
Primary Completion
2016-08-14
Completion
2016-08-14

Countries

  • Russia

More Related Trials

Entities

Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02159261 on ClinicalTrials.gov