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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00737880
Other study ID # CL-KSM-III/6/00
Secondary ID
Status Completed
Phase Phase 4
First received August 19, 2008
Last updated August 19, 2008
Start date July 2001
Est. completion date December 2005

Study information

Verified date August 2008
Source Medical University Innsbruck
Contact n/a
Is FDA regulated No
Health authority Austria: Federal Ministry for Health Family and Youth
Study type Interventional

Clinical Trial Summary

Graft preservation in clinical pancreas transplantation is based on hypothermia achieved by topic cooling and cold in situ flushing using special perfusion solutions designed to attenuate the effects of ischemia/reperfusion and prolong cold ischemia tolerance.

For pancreas transplantation, University of Wisconsin (UW) solution is the most commonly used perfusate. However, over the last years, Histidine-Tryptophan-Ketoglutarate (HTK) solution has been increasingly used for abdominal organ procurement. Retrospective reports published so far have demonstrated the safety of both perfusion solutions.

However, to date, no prospective study comparing both perfusion solutions has been published. Aim of this study was to prospectively evaluate early pancreas graft function in clinical pancreas transplantation after organ perfusion with HTK vs. UW solution.

The study hypothesis is that HTK is not inferior to UW for organ perfusion during procurement in clinical pancreas transplantation.


Recruitment information / eligibility

Status Completed
Enrollment 68
Est. completion date December 2005
Est. primary completion date January 2004
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 60 Years
Eligibility Inclusion Criteria:

- brain dead, heart beating organ donor

- donor age 10 - 50 years

- donor body mass index < 30kg/m2

- pancreas cold ischemia time < 20 hours

- written informed consent of the pancreas recipient

Exclusion Criteria:

- missing written consent

- pancreas retransplantation

- recipient participation in another study

Study Design

Allocation: Randomized, Endpoint Classification: Safety Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Other:
Organ perfusion during pancreas procurement
Usage of UW or HTK perfusion solution during in situ abdominal organ perfusion in multi-organ procurement

Locations

Country Name City State
Austria Center of Operative Medicine / Department of Visceral, Transplant and Thoracic Surgery / Medical University Innsbruck Innsbruck Tyrol
Belgium Department of General, Hepato-Biliary and Transplantation Surgery Gent
Germany Department of General, Visceral and Transplantation Surgery, Charite Campus Virchow Klinikum, Humboldt University Berlin Berlin
Germany Department of General, Vascular, Thoracic and Transplantation Surgery, University of Rostock Rostock

Sponsors (5)

Lead Sponsor Collaborator
Medical University Innsbruck Charite University, Berlin, Germany, Dr. F. Köhler Chemie GmbH, University Hospital, Ghent, University of Rostock

Countries where clinical trial is conducted

Austria,  Belgium,  Germany, 

Outcome

Type Measure Description Time frame Safety issue
Primary Pancreas graft survival 6 months after transplantation Yes
Secondary Serum amylase 6 months after transplantation No
Secondary Serum lipase 6 months after transplantation No
Secondary C-peptide 6 months after transplantation No
Secondary HbA1c 6 months after transplantation No
Secondary Exogenous insulin requirement 6 months after transplantation No
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