CI

At a glance

ClinicalIndex Comparison Record
Phase 3Completed· 402 enrolled
Drug / intervention
Albuterol +2 moredrug
Likely dose
Albuterol (dose not specified)AI-extracted
Key inclusion· 5
  • Age 40 years or older
  • Using a maintenance respiratory medication
  • Diagnosis of asthma and/or COPD
  • No spirometry test in the past 3 years
Key exclusion· 7
  • Unable to perform adequate spirometry
  • Non-English speaking
  • Pregnant
  • Planning to move from Chicago area within the next year

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT03137303
NCT03137303Phase 3Completed

Reducing Diagnostic Error to Improve Patient Safety in COPD and Asthma (REDEFINE Study)

University of Illinois at Chicago·interventional·Posted May 2, 2017·Updated Feb 26, 2024

In Brief

A Phase 3 clinical trial evaluating Spirometry at initial visit, Albuterol, and 1 other intervention for COPD Asthma. Completed, enrolled 402 participants across 2 sites.

Detailed Summary

The purpose of this study is to evaluate the use of spirometry in identifying Diagnostic Error in COPD and Asthma patients.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsCOPD Asthma
CountriesUnited States

Timeline

Phase 3CompletedFinished
201820192020202120222023202420252026
First PostedMay 2, 2017
Enrollment StartJul 1, 2017
Primary CompletionSep 30, 2019
TodayJul 2, 2026
Enrollment to primary: 2.2 yearsPosted 9.2 years ago

Interventions

Spirometry at initial visitdevice

Initial visit for the intervention group, an initial demographics form and health questionnaires. To evaluate the breathing, a pre and post broncho dilator will be performed as well as a spirometry test.

Albuteroldrug

The post broncho dilator spirometry test will be preformed after a breathing medication called Albuterol. Albuterol is used in standard practice for COPD and is commonly used during spirometry.

Spirometry at 12-month follow-updevice

At the end of the 1 year followup, the patient will be scheduled for a pre and post BD spirometry test and undergo the same spirometry protocol as the intervention group.