A Pharmaceopidemiological Study in Patients Who Use Symbicort SMART

NCT00503061 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 1000

Last updated 2010-12-01

No results posted yet for this study

Summary

To investigate how common it is that patients using Symibort SMART take high average daily doses that are not considered appropriate by their physician (overuse) or are hospitalised due to their asthma at least partly due to underuse.

Conditions

  • Bronchial Asthma

Sponsors & Collaborators

Principal Investigators

  • Catriona McMahon, MD · AZ UK MC

  • Tomas Andersson, MD · AZ R&D Lund

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2007-06-30
Primary Completion
2010-05-31
Completion
2010-05-31

Countries

  • United Kingdom

Study Locations

More Related Trials

Entities

Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00503061 on ClinicalTrials.gov