Effects of Intraarterial Octreotide on Pancreatic Texture
Primary Purpose
Pancreatic Fistula
Status
Completed
Phase
Not Applicable
Locations
Germany
Study Type
Interventional
Intervention
Intraarterial application of Octreotide
sterile NaCl (sodium chloride) 0,9% solution
Sponsored by
About this trial
This is an interventional basic science trial for Pancreatic Fistula focused on measuring octreotide, intraarterial, pancreatic hardness, pancreatoduodenectomy, durometer, dynamometer
Eligibility Criteria
Inclusion Criteria:
- age between 18 an 90 years
- planned pancreatoduodenectomy
- signed informed consent
- pancreatic hardness equal or less than 40 SU as measured by durometer
- normal vascular anatomy of the hepato-pancreatic region
Exclusion Criteria:
- planned distal pancreatic resection
- planned non-resectional pancreatic surgery
- acute pancreatitis at the time of surgery
- pancreatic hardness before intervention higher than 40 SU as measured by durometer
- intraoperatively unstable patient
- intraoperative complications
- allergy towards octreotide
- anatomical variation of the vascular supply of the liver or pancreas posing an increased risk for octreotide distribution in other organs than pancreas
- lacking gastroduodenal artery or technically impossible cannulation of the artery
Sites / Locations
- Department of Surgery, St. Josef Hospital, Ruhr University of Bochum
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Placebo Comparator
Arm Label
Octreotide
Control
Arm Description
Study patients receive after randomization a single shot of 5 mL 500 µg Octreotide in the gastroduodenal artery at the time of its transection.
Control patients receive after randomization a single shot of 5 mL 0,9% NaCL solution in the gastroduodenal artery at the time of its transection.
Outcomes
Primary Outcome Measures
Pancreatic hardness
Pancreatic hardness is a quantifiable parameter, measured by a Shore Durometer in Shore Units on a 0-100 SU scale.
Secondary Outcome Measures
Rate of postoperative pancreatic fistula
Postoperative pancreatic fistula occurrs after pancreatoduodenectomy with an estimated rate of 5-30% depending on the definition used and a number of factors such as surgical technique, pancreatic texture, experience of the surgeon, hospital volume etc.
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT01400100
Brief Title
Effects of Intraarterial Octreotide on Pancreatic Texture
Official Title
Changes in Pancreatic Texture After Single-shot Administration of 500 µg Octreotide in the Gastroduodenal Artery During Pancreatoduodenectomy - a Double-Blinded Randomized Controlled Trial
Study Type
Interventional
2. Study Status
Record Verification Date
March 2012
Overall Recruitment Status
Completed
Study Start Date
August 2011 (undefined)
Primary Completion Date
February 2012 (Actual)
Study Completion Date
March 2012 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
St. Josef Hospital Bochum
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
The aim of the study is to test the hypothesis that intraarterial bolus application of 500 µg Octreotide in the gastroduodenal artery during the resectional phase of pancreatoduodenectomy in patients with soft pancreatic tissue hardens the texture of the pancreatic remnant.
A primary end-point of the study is a change in pancreatic texture.
A secondary end-point is the rate of postoperative pancreatic fistula.
Detailed Description
Soft pancreas is an established risk factor for the development of postoperative pancreatic fistula in patients undergoing pancreatoduodenectomy. Octreotide is believed to harden the pancreas. This theory is based on the results of a single animal experiment and a small case series in humans. This hardening effect of octreotide has not quantitatively been proven in humans and its mechanism is not clear. Histomorphologic correlates of pancreatic hardness are unknown.
In this study all patients who are eligible for pancreatoduodenectomy and sign the informed consent for participation in the study will be recruited. Those of them who prove to have a soft pancreas intraoperatively will receive a single bolus of 500 µg Octreotide in the gastroduodenal artery after its proximal division. Pancreatic hardness in the region of the resection margin will be quantitatively assessed by a Shore durometer before the intervention and at several time-points after it. The suture-holding capacity of pancreatic tissue at the resection margin will be quantitatively assessed by a dynamometer. Histomorphological features of pancreatic tissue will be characterized in details at the Institute of Pathology in order to define possible correlates of pancreatic hardness.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Pancreatic Fistula
Keywords
octreotide, intraarterial, pancreatic hardness, pancreatoduodenectomy, durometer, dynamometer
7. Study Design
Primary Purpose
Basic Science
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare Provider
Allocation
Randomized
Enrollment
26 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Octreotide
Arm Type
Experimental
Arm Description
Study patients receive after randomization a single shot of 5 mL 500 µg Octreotide in the gastroduodenal artery at the time of its transection.
Arm Title
Control
Arm Type
Placebo Comparator
Arm Description
Control patients receive after randomization a single shot of 5 mL 0,9% NaCL solution in the gastroduodenal artery at the time of its transection.
Intervention Type
Drug
Intervention Name(s)
Intraarterial application of Octreotide
Other Intervention Name(s)
Sandostatin (Novartis Pharma, Switzerland), Bendatreotid, Octreo, Siroctid, Octreotid
Intervention Description
500 µg / 5 ml Octreotide is given as a single bolus injection in the gastroduodenal artery intraoperatively.
Intervention Type
Drug
Intervention Name(s)
sterile NaCl (sodium chloride) 0,9% solution
Other Intervention Name(s)
Sodium chloride 0,9% solution
Intervention Description
a single intraarterial shot of 5 ml saline solution in the gastroduodenal artery
Primary Outcome Measure Information:
Title
Pancreatic hardness
Description
Pancreatic hardness is a quantifiable parameter, measured by a Shore Durometer in Shore Units on a 0-100 SU scale.
Time Frame
3 months postoperatively
Secondary Outcome Measure Information:
Title
Rate of postoperative pancreatic fistula
Description
Postoperative pancreatic fistula occurrs after pancreatoduodenectomy with an estimated rate of 5-30% depending on the definition used and a number of factors such as surgical technique, pancreatic texture, experience of the surgeon, hospital volume etc.
Time Frame
3 months postoperatively
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
90 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
age between 18 an 90 years
planned pancreatoduodenectomy
signed informed consent
pancreatic hardness equal or less than 40 SU as measured by durometer
normal vascular anatomy of the hepato-pancreatic region
Exclusion Criteria:
planned distal pancreatic resection
planned non-resectional pancreatic surgery
acute pancreatitis at the time of surgery
pancreatic hardness before intervention higher than 40 SU as measured by durometer
intraoperatively unstable patient
intraoperative complications
allergy towards octreotide
anatomical variation of the vascular supply of the liver or pancreas posing an increased risk for octreotide distribution in other organs than pancreas
lacking gastroduodenal artery or technically impossible cannulation of the artery
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Orlin Belyaev, MD
Organizational Affiliation
Department of Surgery, St. Josef Hospital
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Christian Polle
Organizational Affiliation
Ruhr University of Bochum
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Waldemar Uhl, MD, PhD
Organizational Affiliation
Department of Surgery, St. Josef Hospital
Official's Role
Study Chair
Facility Information:
Facility Name
Department of Surgery, St. Josef Hospital, Ruhr University of Bochum
City
Bochum
State/Province
NRW
ZIP/Postal Code
44791
Country
Germany
12. IPD Sharing Statement
Citations:
PubMed Identifier
16568326
Citation
Foitzik T, Gock M, Schramm C, Prall F, Klar E. Octreotide hardens the pancreas. Langenbecks Arch Surg. 2006 Apr;391(2):108-12. doi: 10.1007/s00423-006-0030-z. Epub 2006 Mar 28.
Results Reference
background
PubMed Identifier
15726611
Citation
Konstadoulakis MM, Filippakis GM, Lagoudianakis E, Antonakis PT, Dervenis C, Bramis J. Intra-arterial bolus octreotide administration during Whipple procedure in patients with fragile pancreas: a novel technique for safer pancreaticojejunostomy. J Surg Oncol. 2005 Mar 15;89(4):268-72. doi: 10.1002/jso.20193.
Results Reference
background
PubMed Identifier
19394646
Citation
Belyaev O, Herden H, Meier JJ, Muller CA, Seelig MH, Herzog T, Tannapfel A, Schmidt WE, Uhl W. Assessment of pancreatic hardness-surgeon versus durometer. J Surg Res. 2010 Jan;158(1):53-60. doi: 10.1016/j.jss.2008.08.022.
Results Reference
background
PubMed Identifier
23963030
Citation
Belyaev O, Polle C, Herzog T, Munding J, Chromik AM, Meurer K, Tannapfel A, Bergmann U, Muller CA, Uhl W. Effects of intra-arterial octreotide on pancreatic texture: a randomized controlled trial. Scand J Surg. 2013;102(3):164-70. doi: 10.1177/1457496913490457.
Results Reference
derived
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Effects of Intraarterial Octreotide on Pancreatic Texture
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