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Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT00274222
Other study ID # 2006-3
Secondary ID
Status Terminated
Phase N/A
First received January 9, 2006
Last updated January 9, 2006
Start date January 2003
Est. completion date October 2005

Study information

Verified date January 2006
Source Inonu University
Contact n/a
Is FDA regulated No
Health authority TURKEY: INONU UNIVERSITY PULMONARY MEDICINE
Study type Observational

Clinical Trial Summary

This study was designed to evaluate the hypothesis that nebulized budesonide) might be an alternative to systemic corticosteroids (SC) in the treatment of patients with acute exacerbations of COPD (AECOPD).


Description:

Patients, hospitalized with AECOPD, were randomized into three groups. Group I received only bronchodilator treatment (BDT), Group II received SC (40 mg prednisolon) plus BDT, and Group III received nebulized budesonide (NB)(1500 mcg qid) plus BDT. Improvement rates in multiple parameters during 10-day hospitalization, and acute exacerbation and re-hospitalization rates within one-month after discharge were compared between the groups.


Recruitment information / eligibility

Status Terminated
Enrollment 120
Est. completion date October 2005
Est. primary completion date
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria:

- COPD patients who were admitted to our pulmonary department for an acute exacerbation were prospectively enrolled in the study

Exclusion Criteria:

- COPD patients hospitalized with specific reasons like pneumonia, pulmonary emboli, congestive heart failure, pneumothorax etc. as the cause of acute exacerbation, or patients with risk of imminent respiratory failure requiring mechanical ventilation or direct admission to the ICU were excluded.

Study Design

N/A


Related Conditions & MeSH terms


Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Inonu University
See also
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