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The Nuvigil and Provigil Pregnancy Registry

Obstructive Sleep Apnea Clinical Trial

Official title:
The Nuvigil (Armodafinil) Tablets [C-IV]/Provigil (Modafinil) Tablets [C-IV] Pregnancy Registry

Clinical Trial Summary

The primary objective of the Nuvigil/Provigil Pregnancy Registry is to characterize the pregnancy and fetal outcomes associated with Nuvigil and Provigil exposure during pregnancy.

Clinical Trial Description

Both the prospective and the retrospective data are captured. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01792583
Study type Observational [Patient Registry]
Source Teva Branded Pharmaceutical Products R&D, Inc.
Contact
Status Terminated
Phase
Start date June 30, 2009
Completion date November 30, 2023
View Details
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