MedTrace Logo

Post-marketing, Observational Study to Confirm the Safety and Efficacy of MARVELON (Study P06083)

NCT01005056 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 3838

Last updated 2022-02-04

No results posted yet for this study

Summary

The purpose of this study is to evaluate the efficacy and safety of Marvelon® in the prevention of pregnancy.

Post-marketing surveys are not considered applicable clinical trials and thus the results of this survey will not be posted at its conclusion. The results will be submitted to public health officials as required by applicable national and international laws.

Conditions

  • Contraception

Interventions

DRUG

Ethinylestradiol + Desogestrel

All participants receive Marvelon® according to the approved dosage and administration method.

Sponsors & Collaborators

  • Organon and Co

    lead INDUSTRY

Eligibility

Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2005-05-31
Primary Completion
2009-03-31
Completion
2009-03-31

More Related Trials

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 NCT01005056 on ClinicalTrials.gov