The Use of Surfactant in Lung Transplantation: A Randomized Control Pilot Study

Sponsor
Rabin Medical Center (Other)
Overall Status
Unknown status
CT.gov ID
NCT00506532
Collaborator
(none)
42
1
47
0.9

Study Details

Study Description

Brief Summary

  1. Working Hypothesis:

The purpose of the trial is to study the effect of exogenous calf surfactant (calfactant) on the prevention of primary graft failure due to ischemic-reperfusion lung injury in lung transplant patients.

  1. Aims of the Study:

The purpose of the trial is to study the effect of exogenous calf surfactant (calfactant) on the prevention of primary graft failure due to ischemic-reperfusion lung injury in lung transplant patients.

Condition or Disease Intervention/Treatment Phase
  • Drug: Surfactant (calfactant)
Phase 2/Phase 3

Detailed Description

Background: Lung transplantation induces surfactant dysfunction that may be a contributing factor for primary graft dysfunction (PGD) and graft failure. Animal studies and limited human reports suggest that surfactant administration may prevent primary graft dysfunction.

Working hypothesis and aims:

The purpose of the trial is to study the effect of exogenous calf surfactant (calfactant) on the prevention of primary graft failure due to ischemic-reperfusion lung injury in lung transplant patients.

Methods: The trial is an open randomized controlled prospective study. Patient population: 42 patients eligible for lung transplant according to hospital criteria.

Study medication: Calfactant intratracheal suspension -an extract of natural surfactant from calf lungs, which includes phospholipids, neutral lipids and surfactant-associated proteins B and C (SP-B and SP-C).

Study design: Patients randomized to receive calfactant will have the drug administered through a fiberoptic bronchoscope distributing the drug evenly across the lung immediately after connection. The other patient will not have any administration to avoid any excessive flushing. When 2 lungs will be used from the same donor for 2 recipients one patient receiving one lung will be treated with calfactant while the other patient receiving the other lung will not be treated and serve as the control. Otherwise lungs will be treated with surfactant in every other case.

Expected results: We expect surfactant instillation during lung transplantation to improve oxygenation, prevent primary graft dysfunction, make intubation time shorter and to enhance early post transplantation recovery. In a pilot study that we already performed results are encouraging.

Importance: PGD could cause substantial morbidity and mortality among transplanted patients. In a pilot study we already found that surfactant instillation during lung transplantation improves oxygenation, prevents primary graft dysfunction, shortens intubation time and ICU stay. We believe that surfactant treatment enhances early post transplantation recovery, and may also be cost effective by shortening expensive ICU stay.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
42 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Prevention
Official Title:
The Use of Surfactant in Lung Transplantation: A Randomized Control Pilot Study
Study Start Date :
Jan 1, 2005
Anticipated Study Completion Date :
Dec 1, 2008

Outcome Measures

Primary Outcome Measures

  1. Effect of intraoperative exogenous surfactant treatment on oxygenation and primary graft dysfunction (PGD) prevention (primary outcome) [3 days post operation]

Secondary Outcome Measures

  1. Recovery-Extubation ;Seating time; Icu stay; Hospital stay; Lung function [1 month]

Eligibility Criteria

Criteria

Ages Eligible for Study:
16 Years to 68 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Candidates for lung transplantation
Exclusion Criteria:
  • Differential diagnosis of PGD

  • Pulmonary Edema

  • Stenosis or thrombosis of pulmonary artery/vein anastomosis

Contacts and Locations

Locations

Site City State Country Postal Code
1 Pulmonary Institute Rabin Medical Center Petach Tikva Israel 49100

Sponsors and Collaborators

  • Rabin Medical Center

Investigators

  • Principal Investigator: MordechaI R Kramer, Prof, Pulmonary Institute Rabin Medical Center

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
, ,
ClinicalTrials.gov Identifier:
NCT00506532
Other Study ID Numbers:
  • RMC063344ctil
First Posted:
Jul 25, 2007
Last Update Posted:
Jul 25, 2007
Last Verified:
Jul 1, 2007

Study Results

No Results Posted as of Jul 25, 2007