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COMPLETEDNANCT04347044

The Effect of Pulmonary Rehabilitation on Bronchoscopic Volume Reduction Process Success

The data of patients undergoing bronchoscopic volume reduction procedure will be analyzed retrospectively. Patients will be divided into two groups as patients with and without Pulmonary Rehabilitatio...

Lead sponsor: Istanbul Medipol University Hospital•View source on ClinicalTrials.gov

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Sponsors

Lead Sponsor

Istanbul Medipol University Hospital

The data of patients who underwent bronchoscopic volume reduction between January 2013 and March 2019 will be examined. Patients will be divided into two groups as pulmonary rehabilitation applied (PR group) and not applied (Control group) before the procedure. Changes in the parameters of initial and rehabilitation follow-up will be examined.

Age

18 - 75 years

Sex

ALL

Healthy Volunteers

No

Inclusion Criteria

•Between the ages of 18-75
•Patients with a diagnosis of emphysema and bronchoscopic procedures

Exclusion Criteria

•Patients who develop complications related to the procedure after bronchoscopic procedure.

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Data from ClinicalTrials.govLast updated on ClinicalTrials.gov: August 19, 2020Terms

Trial snapshot

StatusCOMPLETED

PhaseNA

Enrollment80

Start dateJan 2013

Last updatedAug 19, 2020

Condition

Emphysema Pulmonary Rehabilitation Bronchoscopic Lung Volume Reduction

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Data Source & Attribution

This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.

ClinicalTrials.gov last update: August 19, 2020Data synced to Clareo: June 28, 2026

Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.

Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.

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