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

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

Status
UNKNOWN
Phases
Phase 2Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00506532
Enrollment
42
Registered
2007-07-25
Start date
2005-01-31
Completion date
2008-12-31
Last updated
2007-07-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Lung Transplantation, Primary Graft Dysfunction

Keywords

Pulmonary Surfactants, Lung transplantation, Primary Graft Dysfunction

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. 2. 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.

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.

Interventions

DRUGSurfactant (calfactant)

Sponsors

Rabin Medical Center
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
16 Years to 68 Years
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

Design outcomes

Primary

MeasureTime frame
Effect of intraoperative exogenous surfactant treatment on oxygenation and primary graft dysfunction (PGD) prevention (primary outcome)3 days post operation

Secondary

MeasureTime frame
Recovery-Extubation ;Seating time; Icu stay; Hospital stay; Lung function1 month

Countries

Israel

Contacts

Primary ContactMordechai R Kramer, Prof
kremerm@clalit.org.il972-3-9377121
Backup ContactAnat Amital, Dr
anatam@clalit.org.il972-3-9377140

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026