Tolterodine Drug Use Investigation.(Post Marketing Commitment Plan)

Status Completed

Clinical Trial Summary

The objective of this surveillance is to collect information about 1) adverse drug reaction not expected from the Package Insert (unknown adverse drug reaction), 2) the incidence of adverse drug reactions in this surveillance, and 3) factors considered to affect the safety and/or efficacy of this drug.

Clinical Trial Description

All the subjects whom an investigator prescribes the first Detrusitol Capsule should be registered consecutively until the number of subjects reaches target number in order to extract patients enrolled into the investigation at random. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT01488578
Study type	Observational
Source	Pfizer
Contact
Status	Completed
Phase
Start date	December 2006
Completion date	March 2011

View Details

See also
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Tolterodine Drug Use Investigation.(Post Marketing Commitment Plan) — POTTOR

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms