ELVR in PH Patients With Severe Emphysema

NCT ID: NCT01393379

Last Updated: 2015-06-22

Study Results

Results pending

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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Recruitment Status

COMPLETED

Total Enrollment

10 participants

Study Classification

OBSERVATIONAL

Study Start Date

2010-04-30

Study Completion Date

2014-12-31

Brief Summary

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The purpose of this study is to investigate the effect of endoscopic valve implantation in patients with COPD and PH on hemodynamics, symptoms, exercise tolerance and quality of life in 10 patients in a prospective study. An improvement of objective parameters may also have a prognostic significance

Detailed Description

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So far there is no treatment of COPD in addition to the established treatment of concomitant PH. Administration of PH-specific medication outside of clinical trials is not recommended in new guidelines for PH of the ERS/ESC. The influence of endobronchial valve implantation on the PH has not been studied in detail. The purpose of this study is to investigate the effect of endoscopic valve implantation in patients with COPD and PH on hemodynamics, symptoms, exercise tolerance and quality of life in 10 patients in a prospective study. An improvement of objective parameters may also have a prognostic significance

Conditions

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COPD Pulmonary Emphysema

Study Design

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Study Time Perspective

PROSPECTIVE

Eligibility Criteria

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Inclusion Criteria

* signed patient consent form
* men and women \>30 years
* Clinically indicated endoscopic lung volume reduction
* Pulmonary hypertension according to Group 3.1 of the Dana Point classification
* Severe pulmonary emphysema
* FEV1 \<45%
* RV\> 150%
* TLC\> 100%
* Maximum of medical therapy according to GOLD
* heterogeneous emphysema
* Detected in the HR-CT
* Confirmation of the heterogeneity of emphysema by computer-assisted quantification (YACTA ®)
* stable COPD
* No exacerbation in the last 8 weeks
* Cortisone dose \<20 mg prednisolone equivalent
* Non-or ex-smoker
* Nicotine abstinence\> 4 months
* Actual CoHb \<2.5%
* Diagnosis of pulmonary hypertension (PH), invasively diagnosed by right heart catheterization:
* Mean pulmonary arterial pressure (mPAP)\> 25 mmHg
* Pulmonary capillary wedge pressure (PCWP) \<15 mmHg
* Pulmonary vascular resistance (PVR)\> 320 dyne \* sec \* cm-5

Exclusion Criteria

* PH of Group 1, 2, 4, 5 of the Dana Point Classification
* Previous operations
* s/p Lung resection (lobectomy / pneumonectomy)
* s/p endoscopic lung volume resection
* significant bronchiectasis
* Sputum volume\> 4 tablespoons / day
* Severe cardiac comorbidities:
* s/p myocardial infarction in the last 6 weeks
* Congestive heart failure
* Cardiomyopathy with highly impaired LVF
* Clopidogrel in long-term medication
* Respiratory insufficiency: PaCO2 mmHg at rest\> 55
* current pregnancy
Minimum Eligible Age

30 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Heidelberg University

OTHER

Sponsor Role lead

Responsible Party

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Prof. Dr. med. Ekkehard Gruenig

Prof. Grünig / PD Dr. Eberhardt

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Christoph Corvinus, MD

Role: PRINCIPAL_INVESTIGATOR

Center for pulmonary hypertension, Thoraxclinic Heidelberg

Locations

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Center for pulmonary Hypertension, Thoraxclinic Heidelberg

Heidelberg, , Germany

Site Status

Countries

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Germany

Other Identifiers

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S445/2009

Identifier Type: -

Identifier Source: org_study_id

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