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Endoscopic Lung Volume Reduction Coil Treatment in Patients With Chronic Hypercapnic Respiratory Failure

Terminated
Conditions
Emphysema
Registration Number
NCT02996149
Lead Sponsor
Universitätsklinikum Hamburg-Eppendorf
Brief Summary

Endoscopic lung volume reduction coil treatment is a treatment option for selected patients with severe emphysema. In the advanced stages, emphysema may lead to chronic hypercapnic respiratory failure. In this observational study the safety and efficacy of endoscopic lung volume reduction coil treatment in patients with chronic hypercapnic respiratory failure is evaluated.

Detailed Description

Not available

Recruitment & Eligibility

Status
TERMINATED
Sex
All
Target Recruitment
1
Inclusion Criteria
  • Patients with emphysema (chronic obstructive pulmonary disease with forced expired volume in one second (FEV1) < 50% predicted and residual volume (RV) ≥ 200% predicted) in whom endoscopic lung volume reduction coil treatment is performed
  • Chronic hypercapnic respiratory failure (PaCO2 ≥ 50 mmHg)
  • Informed consent
Exclusion Criteria
  • Therapeutic anticoagulation
  • Anti-platelet therapy exceeding the use of acetylsalicylic acid
  • Severe pulmonary hypertension

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Changes in PaCO23 months after endoscopic lung volume reduction (ELVR)
Secondary Outcome Measures
NameTimeMethod
Changes in PaCO26 and 12 months after ELVR
Changes in FEV13, 6 and 12 months after ELVR
Changes in vital capacity3, 6 and 12 months after ELVR
Changes in residual volume3, 6 and 12 months after ELVR
Changes in 6-minute walk distance3, 6 and 12 months after ELVR
Changes in quality of life (St. George's Respiratory Questionnaire, SGRQ)3, 6 and 12 months after ELVR
Changes in BMI3, 6 and 12 months after ELVR

Trial Locations

Locations (1)

University Hospital Hamburg-Eppendorf

🇩🇪

Hamburg, Germany

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