Observational Trial With Leios/Alesse

A prospective, observational study (Anwendungsbeobachtung [AWB]) of the prescribing and administration practices of German gynecologists with Leios® Dragées...

Date First Received: May 31, 2007

Last Updated: December 7, 2007

Verified by: Wyeth, December 2007

Clinical Trial Phase: Phase 4 | Start Date: May 2005

Overall Status: Completed

Brief Summary

Official Title: “A Prospective Observation Study (Anwendungsbeobachtung [AWB]) of the Prescribing and Administration Practices of German Gynecologists With Leios® Dragées/Alesse”

Condition Keyword(s):

Intervention(s):

A prospective, observational study (Anwendungsbeobachtung [AWB]) of the prescribing and administration practices of German gynecologists with Leios® Dragées.

Study Type: Observational

Study Design: Prospective

Intervention(s) in this Clinical Trial

  • Drug: Leios/Alesse

Criteria for Participation in this Clinical Trial

Inclusion Criteria:

  • Healthy, women, aged under 40

Gender Eligibility for this Clinical Trial: Female

Minimum Age for this Clinical Trial: N/A

Maximum Age for this Clinical Trial: 40 Years

Are Healthy Volunteers Accepted for this Clinical Trial?: Accepts Healthy Volunteers

Clinical Trial Sponsor Information

Lead Sponsor: Wyeth

Overall Clinical Trial Officials and Contacts

Medical Monitor Study Director Wyeth  

Additional Information

Information obtained from ClinicalTrials.gov on September 04, 2008

Link to the current ClinicalTrials.gov record. http://clinicaltrials.gov/show/NCT00481650

Study ID Number: 101742

ClinicalTrials.gov Identifier: NCT00481650

Health Authority: Germany: Federal Institute for Drugs and Medical Devices

Clinical Trials Authorship and Review

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