Clinical Trials Directory

Trials / Completed

CompletedNCT00998309

Zithromax-SR 2g, Special Investigation (Regulatory Post Marketing Commitment Plan)

Zithromax-SR 2g, Special Investigation For Skin And Soft Tissue Infection, Sexually-Transmitted Infection, And Infection Of The Oral (Regulatory Post Marketing Commitment Plan)

Status
Completed
Phase
Study type
Observational
Enrollment
502 (actual)
Sponsor
Pfizer · Industry
Sex
All
Age
Healthy volunteers
Not accepted

Summary

To collect the efficacy and safety information of Zithromax-SR related to their appropriate use in daily practice.

Detailed description

All the patients whom an investigator prescribes the first Azithromycin SR should be registered within 14 days.

Conditions

Interventions

TypeNameDescription
DRUGAzithromycin SRZithromax SR 2g, taking once for treatment.

Timeline

Start date
2009-10-01
Primary completion
2011-01-01
Completion
2011-01-01
First posted
2009-10-20
Last updated
2012-05-01
Results posted
2012-05-01

Source: ClinicalTrials.gov record NCT00998309. Inclusion in this directory is not an endorsement.

Zithromax-SR 2g, Special Investigation (Regulatory Post Marketing Commitment Plan) (NCT00998309) · Clinical Trials Directory