Pancreas Transplantation Clinical Trial
Official title:
Effects of Goal-Directed Therapy on Inflammatory Mediators and Postoperative Outcome in Pancreas Transplant: a Prospective Randomised Clinical Trial
A Pancreas Transplant is the accepted treatment in patients with Insulin Dependent Diabetes
Mellitus (IDDM) and end-organ failure. Simultaneous Pancreas and Kidney (SPK) Transplant is
done in over 90% of cases. At present there is a 5- 8% 30-day mortality with over 80% graft
survival at 1 year. At Manchester Royal Infirmary (MRI) approximately 40 cases are done per
year.
Goal-Directed Therapy (GDT) involves fluid resuscitation intra-operatively and early in the
post-operative period, guided by cardiac output monitoring. The mechanism of therapeutic
benefit is thought to be related to improved tissue oxygenation and oxygen delivery. There
are a number of studies showing significantly improved biochemical markers of inflammation
in animal models and in studies on septic patients (patients with an overwhelming infection)
following GDT. Studies have also shown that GDT improves clinical outcome in post-operative
patients and in serum inflammatory mediators. These studies have looked at "major abdominal
surgery" but none have investigated transplant patients. Given the nature of surgery we feel
that our patients would benefit with reduced Intensive Care Unit stay, reduced length of
hospital stays and reduced rates of post-operative complications.
The study will be conducted on all adult patients undergoing pancreas transplant at MRI. It
will last for 2 years and we hope to recruit 60 patients
Patients will be randomised into Standard Therapy (ST) or GDT groups, with ST being current
practice. Each intervention will last for six hours post-operatively before continuing with
normal care thereafter. Omental fat biopsies will be taken from patients intra-operatively
and blood samples will be taken from patients at regular intervals for 72 hours intra- and
post- operatively. Patients will be followed up daily while an in-patient and at
three-monthly intervals in out-patients for 1 year.
n/a
Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment
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