Islet Autotransplantation in Patients at Very High-risk Pancreatic Anastomosis (PAN-IT)
Primary Purpose
Postpancreatectomy Hyperglycemia
Status
Completed
Phase
Phase 2
Locations
Italy
Study Type
Interventional
Intervention
Pancreaticoduodenectomy with pancreatic anastomosis
Total pancreatectomy with islet autotransplantation
Sponsored by
About this trial
This is an interventional treatment trial for Postpancreatectomy Hyperglycemia focused on measuring diabetes, islet transplantation, pancreas, pancreatectomy
Eligibility Criteria
Inclusion Criteria:
- Patients >18 years of age
- Ability to provide written informed consent
- Mentally stable and able to comply with the procedures of the study protocol
- Fasting glycaemia <126 mg/dl without glucose-lowering medications.
Exclusion Criteria:
- Any medical condition that, in the opinion of the investigator, will interfere with the safe completion of the trial
- Diagnosis of intraductal papillary mucinous cancer, unless the absence of multifocal lesion is demonstrated by endoscopic US
- Presence of multifocal or residual disease at the pancreatic margin.
Sites / Locations
- IRCCS San Raffaele
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
GROUP B
GROUP A
Arm Description
At the time of surgery the surgeon will directly assess pancreatic consistency and the pancreatic duct size. In the presence of a soft pancreas and a small duct (diameter <3 mm), the patient will be randomly assigned to receive either a pancreaticoduodenectomy with pancreatic anastomosis (group A) or a total pancreatectomy with IAT (group B).
Outcomes
Primary Outcome Measures
incidence of complications after pancreatic surgery
Complications will be defined and graded according to the Novel Grading System classification ( DeOliveira et al 2006). A special emphasis is given to life-threatening and permanently disabling complications.
Secondary Outcome Measures
Incidence of each individual postoperative complication
death
pancreatic fistula defined according to the International Study Group on Pancreatic Fistula (Bassi C et al 2005)
delayed gastric emptying (DGE) defined according to the International Study Group on Pancreatic Fistula (Wente et al 2007)
intra-abdominal complications
medical complications
Incidence of endocrine and exocrine pancreatic insufficiency
We will assess endocrine pancreatic function by measuring fasting plasma glucose and HbA1c in all patients.
Clinical hallmarks of pancreatic exocrine insufficiency include symptoms of fat malabsorption, such as steatorrhea, weight loss and abdominal pain. Frequency of bowel movements and characteristics of stools will be serially recorded. Fat-soluble vitamins such as A, D, E and K will be measured 12 month after the hospital discharge after the index surgery. Oral pancreatic enzyme supplementation will be prescribed according to the severity of clinical steatorrhea and weight loss.
Full Information
NCT ID
NCT01346098
First Posted
April 29, 2011
Last Updated
November 2, 2020
Sponsor
Ospedale San Raffaele
Collaborators
Ministry of education, university and research, Italy
1. Study Identification
Unique Protocol Identification Number
NCT01346098
Brief Title
Islet Autotransplantation in Patients at Very High-risk Pancreatic Anastomosis
Acronym
PAN-IT
Official Title
Total Pancreatectomy With Islet Autotransplantation as a Superior Alternative to Pancreatoduodenectomy in Patients at Very High-risk of Complications of the Pancreatic Anastomosis: a Single-center Prospective Randomised Clinical Trial
Study Type
Interventional
2. Study Status
Record Verification Date
November 2020
Overall Recruitment Status
Completed
Study Start Date
July 2010 (Actual)
Primary Completion Date
December 2018 (Actual)
Study Completion Date
April 2019 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Ospedale San Raffaele
Collaborators
Ministry of education, university and research, Italy
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
The goal of the proposal is to demonstrate that, in patients with disease of the pancreatic head with very high-risk of complications of pancreatojejunal reconstruction (soft pancreas and pancreatic duct diameter <3 mm), total pancreatectomy with islet autotransplantation (IAT) is associated with a lower morbidity (in terms of surgical or medical complications) and mortality compared with pancreaticoduodenectomy and pancreatojejunal anastomosis.
Detailed Description
Complications of the pancreatic anastomosis still represents a significant risk for death after the resection of the pancreatic head. In an effort to decrease morbidity and mortality, the referral of patients who need a pancreaticoduodenectomy to institutions (and surgeons) performing a high volume of this surgical procedure has been championed. Nonetheless, the role of prophylactic medications and the best surgical technique(s) for the removal of the pancreatic head are still debated. However, very few prospective randomized clinical trials have been conducted to compare different surgical techniques.
Our study will address for the first time the role for preemptive total pancreatectomy and IAT in selected patients undergoing pancreaticoduodenectomy that are considered high risk for pancreaticojejunostomy disruption (eg, small pancreatic duct, soft pancreas). The information expected is the identification of total pancreatectomy and the IAT as the standard treatment in a subgroup of patient with pathologies of the pancreatic head at high risk for leakage of pancreatic anastomosis. Ultimately this project will lead to reserve more innovative cell therapy for patients with the highest risk of anastomosis failure reducing pancreatojejunal reconstruction related morbidity and mortality
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Postpancreatectomy Hyperglycemia
Keywords
diabetes, islet transplantation, pancreas, pancreatectomy
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
60 (Actual)
8. Arms, Groups, and Interventions
Arm Title
GROUP B
Arm Type
Experimental
Arm Description
At the time of surgery the surgeon will directly assess pancreatic consistency and the pancreatic duct size. In the presence of a soft pancreas and a small duct (diameter <3 mm), the patient will be randomly assigned to receive either a pancreaticoduodenectomy with pancreatic anastomosis (group A) or a total pancreatectomy with IAT (group B).
Arm Title
GROUP A
Arm Type
Active Comparator
Intervention Type
Procedure
Intervention Name(s)
Pancreaticoduodenectomy with pancreatic anastomosis
Intervention Description
Standard lymphadenectomy, end-to-side two-layer pancreaticojejunostomy and duodenojejunostomy will be performed. If the pylorus is preserved, so will be the right gastric artery, unless the artery is damaged or hindering adequate gastric mobilization. No prokinetic agent will be administered routinely, but IV metoclopramide will given on demand (10 mg , three times daily). Prophylaxis will consist of octreotide (0,1 mg three times daily from day 0 to 7), low molecular weight heparin and a single dose of antibiotic (cefazolin 2 g). Early postoperative analgesia will be achieved by epidural or, when contraindicated, patient-controlled analgesia
Intervention Type
Procedure
Intervention Name(s)
Total pancreatectomy with islet autotransplantation
Intervention Description
If the patient will be assigned to this group, the surgeon will complete the pancreatectomy preserving the spleen. The body and tail of the pancreas will be sent to the islet isolation facility. Islets will be isolated and purified according to the automated method described by Ricordi. The resulting islet tissue will be suspended in a cold isotonic saline solution and infused into the portal vein during the next 24h.
Primary Outcome Measure Information:
Title
incidence of complications after pancreatic surgery
Description
Complications will be defined and graded according to the Novel Grading System classification ( DeOliveira et al 2006). A special emphasis is given to life-threatening and permanently disabling complications.
Time Frame
90 days from discharge
Secondary Outcome Measure Information:
Title
Incidence of each individual postoperative complication
Description
death
pancreatic fistula defined according to the International Study Group on Pancreatic Fistula (Bassi C et al 2005)
delayed gastric emptying (DGE) defined according to the International Study Group on Pancreatic Fistula (Wente et al 2007)
intra-abdominal complications
medical complications
Time Frame
90 days from discharge
Title
Incidence of endocrine and exocrine pancreatic insufficiency
Description
We will assess endocrine pancreatic function by measuring fasting plasma glucose and HbA1c in all patients.
Clinical hallmarks of pancreatic exocrine insufficiency include symptoms of fat malabsorption, such as steatorrhea, weight loss and abdominal pain. Frequency of bowel movements and characteristics of stools will be serially recorded. Fat-soluble vitamins such as A, D, E and K will be measured 12 month after the hospital discharge after the index surgery. Oral pancreatic enzyme supplementation will be prescribed according to the severity of clinical steatorrhea and weight loss.
Time Frame
12 months after surgery.
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Patients >18 years of age
Ability to provide written informed consent
Mentally stable and able to comply with the procedures of the study protocol
Fasting glycaemia <126 mg/dl without glucose-lowering medications.
Exclusion Criteria:
Any medical condition that, in the opinion of the investigator, will interfere with the safe completion of the trial
Diagnosis of intraductal papillary mucinous cancer, unless the absence of multifocal lesion is demonstrated by endoscopic US
Presence of multifocal or residual disease at the pancreatic margin.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Lorenzo Piemonti, MD
Organizational Affiliation
Fondazione Centro San Raffaele del Monte Tabor
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Gianpaolo Balzano, MD
Organizational Affiliation
Fondazione Centro San Raffaele del Monte Tabor
Official's Role
Study Director
Facility Information:
Facility Name
IRCCS San Raffaele
City
Milan
ZIP/Postal Code
20132
Country
Italy
12. IPD Sharing Statement
Learn more about this trial
Islet Autotransplantation in Patients at Very High-risk Pancreatic Anastomosis
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