Full Text View
Tabular View
No Study Results Posted
Related Studies
Can Aprotinin Reduce Pancreatitis After Scoliosis Surgery
This study is currently recruiting participants.
Verified by Nemours Children's Clinic, February 2009
First Received: July 26, 2006   Last Updated: February 3, 2009   History of Changes
Sponsored by: Nemours Children's Clinic
Information provided by: Nemours Children's Clinic
ClinicalTrials.gov Identifier: NCT00357851
  Purpose

Pancreatitis is caused by an acute injury on the pancreas. This illness is associated with abdominal pain, vomiting or even fever. We have recently reported a high rate of acute pancreatitis developing in children who undergo posterior spinal fusion for scoliosis (to correct spinal curve). We showed that the amount of blood loss during the surgery is related to the incidence of pancreatitis. In addition, some markers that monitor tissue injury are elevated after the surgery and significantly higher in the patients who develop acute pancreatitis later. We propose that if blood loss and tissue injury could be reduced, then the incidence of pancreatits may be less in these children. Therefore we plan to use a drug Aprotinin to just do that.

Aprotinin has been used to reduce blood loss in patients undergoing posterior spinal surgery, the same population we propose to study. If it turns out that Aprotinin can reduce blood loss or/and the damage to the pancreas, thus pancreatitis, it will diminish the pain and discomfort, and shorten hospital stay in these children. The results from this study will guide medical care in these children in the future.


Condition Intervention Phase
Pancreatitis
Drug: Aprotinin
Phase I

MedlinePlus related topics: Scoliosis Surgery
Drug Information available for: Aprotinin
U.S. FDA Resources
Study Type: Interventional
Study Design: Prevention, Randomized, Double-Blind, Placebo Control, Single Group Assignment, Safety/Efficacy Study

Further study details as provided by Nemours Children's Clinic:

Primary Outcome Measures:
  • Blood loss and the incidence of pancreatitis

Secondary Outcome Measures:
  • Ischemic injury

Estimated Enrollment: 120
Study Start Date: March 2005
Detailed Description:

We have shown an association between high intraoperative blood loss in children and young adults undergoing posterior spinal fusion and a subsequent clinical course characterized by a high rate of acute pancreatitis - a rare illness in children. Other complications include sepsis, deep wound infections, and prolonged length of stay. Although it has been reported in children and young adults with idiopathic scoliosis we have shown a significantly higher blood loss and rate of pancreatitis in patients with neuromuscular scoliosis, especially in cerebral palsy. The purpose of this study is to assess the efficacy of Aprotinin, a serine protease inhibitor, in reducing intraoperative blood loss and subsequent clinical pancreatitis and other associated complications in patients with cerebral palsy who undergo posterior spinal fusion. Aprotinin is currently approved for use in adults to reduce major blood loss during cardiac surgery, and it is used in children at virtually all major pediatric cardiac centers. In these populations, blood loss is consistently diminished by 50%. Safety and efficacy in adults and children is well documented, and use of this drug is familiar to most anesthesiologists. In addition, it has been shown to reduce blood loss effectively in large controlled-studies in adults who undergo major orthopedic surgeries, including spinal fusion. Recently one published study has also suggested that Aprotinin may reduced blood loss in children undergoing idiopathic scoliosis surgery, but the study did not have the adequately statistical power due to a small sample size. Since intraoperative blood loss and cytokine elevations are significantly correlated with the incidence of acute pancreatitis, we hypothesize a major role for ischemic injury in the development of pancreatitis and other complications. We expect that Aprotinin by reducing blood loss will prevent ischemic injury hence, decrease the incidence of acute pancreatitis in these children and young adults. While safety and efficacy have been established for cardiac surgery in adults and children, we propose to conduct a double-blind, randomized trial of Aprotinin in children with cerebral palsy who undergo posterior spinal fusion surgery to answer the following specific questions. Specific Aim 1: To assess whether intraoperative Aprotinin infusion can reduce intraoperative blood loss, and whether this lowers the incidence of postoperative pancreatitis and associated complications of sepsis, wound infection and prolonged length of stay.

Specific Aim 2: To assess by indirect methods whether Aprotinin infusion can alter the degree of ischemic injury concomitantly with the reduction of blood loss and the incidence of postoperative pancreatitis.

  Eligibility

Ages Eligible for Study:   up to 18 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

Children of all ages (<18 yr or 18 yr), both boys and girls who undergo posterior spinal fusion with cebebral palsy or neuromuscular scoliosis.

Exclusion Criteria:

  • received Aprotinin previously
  • have severe allergic reaction to medicine
  • received whole blood transfusions
  • bleeding disorder
  • impaired renal function, liver or kidney impairment
  • previous pancreatitis
  • girls who are pregnant.
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00357851

Locations
United States, Delaware
Alfred I. duPont Hospital for Children Recruiting
Wilmington, Delaware, United States, 19803
Contact: Zhaoing He, Ph.D     302-651-6853 ext 302 651 6881     zhe@nemours.org    
Contact: Devendra I Mehta, M.D.     407 650 7041 ext 650 0751     dmehta@nemours.org    
Principal Investigator: Devendra I Mehta, M.D.            
Sub-Investigator: Zhaoping He, Ph.D.            
Sponsors and Collaborators
Nemours Children's Clinic
  More Information

No publications provided

Study ID Numbers: IRB#2003-029
Study First Received: July 26, 2006
Last Updated: February 3, 2009
ClinicalTrials.gov Identifier: NCT00357851     History of Changes
Health Authority: United States: Food and Drug Administration

Keywords provided by Nemours Children's Clinic:
pancreatitis, blood loss

Study placed in the following topic categories:
Serine Proteinase Inhibitors
Scoliosis
Digestive System Diseases
Pancreatic Diseases
Hemorrhage
Hemostatics
Pancreatitis
Protease Inhibitors
Aprotinin

Additional relevant MeSH terms:
Serine Proteinase Inhibitors
Molecular Mechanisms of Pharmacological Action
Coagulants
Hematologic Agents
Enzyme Inhibitors
Pharmacologic Actions
Hemostatics
Aprotinin
Protease Inhibitors
Digestive System Diseases
Therapeutic Uses
Trypsin Inhibitors
Pancreatic Diseases
Pancreatitis

ClinicalTrials.gov processed this record on May 07, 2009