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Observational Trial With Leios/Alesse
This study has been completed.
Study NCT00481650   Information provided by Wyeth
First Received: May 31, 2007   Last Updated: December 7, 2007   History of Changes

May 31, 2007
December 7, 2007
May 2005
 
 
 
Complete list of historical versions of study NCT00481650 on ClinicalTrials.gov Archive Site
 
 
 
Observational Trial With Leios/Alesse
A Prospective Observation Study (Anwendungsbeobachtung [AWB]) of the Prescribing and Administration Practices of German Gynecologists With Leios® Dragées/Alesse

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

 
Phase IV
Observational
Prospective
Contraceptives, Oral, Combined
Drug: Leios/Alesse
 
 

*   Includes publications given by the data provider as well as publications identified by National Clinical Trials Identifier (NCT ID) in Medline.
 
Completed
 
March 2007
 

Inclusion Criteria:

  • Healthy, women, aged under 40
Female
up to 40 Years
Yes
Contact information is only displayed when the study is recruiting subjects
 
 
NCT00481650
 
101742
Wyeth
 
Study Director: Medical Monitor Wyeth
Principal Investigator: Trial Manager For Germany, medinfoDEU@wyeth.com
Wyeth
December 2007

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