The Effect of Pulmonary Rehabilitation on Bronchoscopic Volume Reduction Process Success
NCT ID: NCT04347044
Last Updated: 2020-08-19
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
80 participants
INTERVENTIONAL
2013-01-01
2020-08-18
Brief Summary
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Detailed Description
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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.
Conditions
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Study Design
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NON_RANDOMIZED
PARALLEL
TREATMENT
NONE
Study Groups
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Pulmonary Rehabilitation Group
Optimal medication and clinical follow-up plus Pulmonary rehabiltation
Pulmonary Rehabilitation
Exercise training+ Optimal medication and clinical follow-up
Standart care
Optimal medication and clinical follow-up
Non-Pulmonary Rehabilitation Group
Optimal medication and clinical follow-up
Standart care
Optimal medication and clinical follow-up
Interventions
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Pulmonary Rehabilitation
Exercise training+ Optimal medication and clinical follow-up
Standart care
Optimal medication and clinical follow-up
Eligibility Criteria
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Inclusion Criteria
* Patients with a diagnosis of emphysema and bronchoscopic procedures
Exclusion Criteria
18 Years
75 Years
ALL
No
Sponsors
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Istanbul Medipol University Hospital
OTHER
Responsible Party
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esra pehlivan
Principle investigator
Other Identifiers
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BLVR_PR
Identifier Type: -
Identifier Source: org_study_id
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