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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT03282526
Other study ID # PFTs in COPD
Secondary ID
Status Not yet recruiting
Phase N/A
First received August 26, 2017
Last updated September 12, 2017
Start date September 30, 2017
Est. completion date December 2018

Study information

Verified date August 2017
Source Assiut University
Contact AZZA BAHAA EL-DIN ALI
Phone 01090078962
Email zozo8928@yahoo.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

- Assess the differences between flow and volume responses after bronchodilator reversibility testing in patients over different clinical chronic obstructive pulmonary disease stages (GOLD stage I to GOLD stage IV).

- Study the Correlation between the bronchodilator response and the severity of the disease.


Description:

chronic obstructive pulmonary disease is a common preventable and treatable disease characterized by persistent airflow limitation that is usually progressive. The diagnosis requires an evidence of obstructive pattern by spirometry measured before and after bronchodilators.

The degree of reversibility of airflow obstruction differs between patients, and does not predict the response to bronchodilator therapy. It can be seen in terms of forced vital capacity (FVC) or forced expiratory volume in the first second (FEV1),or Inspiratory capacity (IC) or residual volume (RV).


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 100
Est. completion date December 2018
Est. primary completion date September 2018
Accepts healthy volunteers No
Gender All
Age group 40 Years to 60 Years
Eligibility Inclusion Criteria:

- Patients Clinical diagnosis of Chronic Obstructive Pulmonary Disease

- Must be able to do pulmonary function test

- Age more than 40 years

- Stable Chronic Obstructive Pulmonary Disease patients

Exclusion Criteria:

Any patients with a diagnosis of:

- Bronchial asthma

- Bronchiectasis

- Respiratory failure

- Decompensated core pulmonale

- Chronic Obstructive Pulmonary Disease combined with any other respiratory disease

Study Design


Related Conditions & MeSH terms


Intervention

Diagnostic Test:
Whole body plethysmography
Whole body plethysmography : measure lung volumes Spirometry : to assess severity of chronic obstructive pulmonary disease also reversibility testing

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Assiut University

References & Publications (2)

"Global Strategy for the Diagnosis, Management, and Prevention of Chronic Obstructive Lung Disease 2017 Report: GOLD Executive Summary." Claus F. Vogelmeier, Gerard J. Criner, Fernando J. Martinez, Antonio Anzueto, Peter J. Barnes, Jean Bourbeau, Bartolom — View Citation

Vogelmeier CF, Criner GJ, Martínez FJ, Anzueto A, Barnes PJ, Bourbeau J, Celli BR, Chen R, Decramer M, Fabbri LM, Frith P, Halpin DMG, Varela MVL, Nishimura M, Roche N, Rodríguez-Roisin R, Sin DD, Singh D, Stockley R, Vestbo J, Wedzicha JA, Agustí A. Erra — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Assess the response pattern to inhaled short acting B2 agonist Assess the response pattern to inhaled short acting B2 agonist through measuring flow and volume parameters to define the differences between volumes responders and flow responders twice per day one before inhaled short acting B2 agonist and one after 10 minutes from inhaled short acting B2 agonist for average of 2 year
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