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Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT01357460
Other study ID # Protocol D2.0 - 31.08.2010
Secondary ID
Status Terminated
Phase N/A
First received
Last updated
Start date May 2011
Est. completion date December 30, 2014

Study information

Verified date August 2022
Source Heidelberg University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Patients with advanced heterogeneous emphysema due to alpha1 antitrypsin deficiency might benefit from endoscopic implantation of intrabronchial valves.


Description:

Patient enrollment and data acquisition is to be carried out on a prospective basis. It is planned to enroll a total of 25 patients with advanced heterogeneous emphysema due to alpha1 antitrypsin deficiency. All patients will undergo treatment at one study centre in Heidelberg. Therapy of all patients consists of implantation of intrabronchial valves (IBV, Spiration, Olympus) in the most emphysematous destroyed lobe.


Recruitment information / eligibility

Status Terminated
Enrollment 18
Est. completion date December 30, 2014
Est. primary completion date September 24, 2014
Accepts healthy volunteers No
Gender All
Age group 30 Years and older
Eligibility Inclusion Criteria: - pulmonary function: FEV1 < 45 %, RV > 150 %, TLC > 100 % - alpha1 antitrypsin deficiency (< 80 mg/dl), genotype: PiZS, PiZZ, Pi0/0 - heterogenous emphysema Exclusion Criteria: - homogenous emphysema - significant bronchiectasis - severe concomitant diseases - pregnancy

Study Design


Related Conditions & MeSH terms


Intervention

Device:
Implantation of intrabronchial valves (IBV) (Spiration IBV)
In advanced emphysema due to alpha1 antitrypsin deficiency even optimum treatment including drugs, physical training and possibly oxygen therapy is unable to influence exercise dyspnoea and exercise capacity.Implantation of intrabronchial valves in the most destroyed and hyperinflated lung lobe can improve the elastic recoil of the small airways by a reduction in lung volume and thus leading to more ergonomic breathing mechanics and diaphragm function.The one-way mechanism of these valves allows air to escape from the downstream lung segment without any influx of "new" air during inspiration.

Locations

Country Name City State
Germany Thoraxklinik Heidelberg

Sponsors (1)

Lead Sponsor Collaborator
Heidelberg University

Country where clinical trial is conducted

Germany, 

Outcome

Type Measure Description Time frame Safety issue
Primary Improvement in pulmonary function (FEV1 (forced expiratory volume in 1 second) and RV/TLC (residual volume/total lung capacity) 3 months
Secondary Number of major complications 3 months
Secondary Evaluation of IBV migration rate 3 months
Secondary Average changes in pulmonary function (FEV1, VC (vital capacity), RV, TLC, RV/TLC) 3 months
Secondary Average changes in 6-minute-walk-distance 3 months