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Chronic Pancreatitis. Effect of Pioglitazone on Endocrine Function, Exocrine Function & Structure, Pain & Life Quality

Primary Purpose

Chronic Pancreatitis, Insulin Resistance, Normal or Mildly Abnormal Stool Fat Levels

Status
Completed
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
Pioglitazone
Placebo
Sponsored by
University of Michigan
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Chronic Pancreatitis focused on measuring Chronic pancreatitis, Insulin resistance

Eligibility Criteria

18 Years - 75 Years (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Insulin resistance or mild diabetes mellitus
  • Symptoms of abdominal pain
  • Xray test showing damage to the pancreas
  • Normal or mildly abnormal stool fat levels

Exclusion Criteria:

  • Mentally disabled patients
  • Women who are planning pregnancy, pregnant or lactating/nursing
  • Chronic pancreatitis is due to other specific conditions

    • Autosomal dominant pancreatitis
    • Classic cystic fibrosis with lung involvement
    • Autoimmune pancreatitis
    • Pancreatic cancer
    • Biliary obstruction (non-pancreatic cause)
    • Abdominal trauma
    • Hypercalcemia
    • Hypertriglyceridemia
  • Surgical resection of the head of the pancreas
  • Alcohol consumption within prior 2 months
  • Specific medical conditions

    • Gastric surgery
    • Celiac sprue
    • Crohns disease
    • Heart failure
    • Kidney failure
    • Cirrhosis or liver disease
    • Osteoporosis
    • Blood clotting disorder
    • Visual problems
    • Low albumin
    • Low BMI
  • Specific medications *Diabetes drug treatment is allowed except for short-acting insulin, long-acting insule more than 15 units daily, pioglitazone, rosiglitazone, orlistat, acarbose, miglitol or voglibose.

Sites / Locations

  • University of Michigan Health System

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Placebo Comparator

Arm Label

Pioglitazone

sugar pill (placebo)

Arm Description

30 mg pioglitazone (Actos) tablet taken once daily for 48 weeks.

1 sugar pill (placebo) taken once daily for 48 weeks.

Outcomes

Primary Outcome Measures

Glucose Tolerance at 24 Weeks
Normal = normal plasma glucose and normal glucose tolerance (OGTT). Impaired category includes all non-diabetic participants with either a) Impaired fasting glucose = fasting plasma glucose >110 mg/dl and <126 mg/dl; or b) Impaired glucose intolerance = 2-hour plasma glucose (OGTT) >140 mg/dl and <200 mg/dl. Diabetes = fasting plasma glucose >126 mg/dl 2-hour (OGTT) plasma glucose >200 mg/dl.
Glucose Tolerance at 48 Weeks
Normal = normal plasma glucose and normal glucose tolerance (OGTT). Impaired category includes all non-diabetic participants with either a) Impaired fasting glucose = fasting plasma glucose >110 mg/dl and <126 mg/dl; or b) Impaired glucose intolerance = 2-hour plasma glucose (OGTT) >140 mg/dl and <200 mg/dl. Diabetes = fasting plasma glucose >126 mg/dl 2-hour (OGTT) plasma glucose >200 mg/dl.
Insulin Sensitivity Index for Glycemia at 24 Weeks
Insulin Sensitivity = Index for Glycemia (ISI gly) = 2 / ([INSp x GLYp] + 1). GLYp = Glycemic 0-2 hr area = sum of normalized (based on institutional values) 0 & 2 hr glucose. INSp = Insulinemic 0-2 hr area = sum of normalized (based on institutional values) 0 & 2 hr insulin.
Insulin Sensitivity Index for Glycemia at 48 Weeks.
Insulin Sensitivity = Index for Glycemia (ISI gly) = 2 / ([INSp x GLYp] + 1). GLYp = Glycemic 0-2 hr area = sum of normalized (based on institutional values) 0 & 2 hr glucose. INSp = Insulinemic 0-2 hr area = sum of normalized (based on institutional values) 0 & 2 hr insulin.

Secondary Outcome Measures

Beta-cell Function
Homeostasis model assessment (HOMA 2) values generated using calculator at https://www.dtu.ox.ac.uk/homacalculator/
Insulin Resistance at 24 and 48 Weeks
Homeostasis model assessment (HOMA 2) values generated using calculator at https://www.dtu.ox.ac.uk/homacalculator/
Pancreas Ultrasound Appearance
Mean score on a scale of 0 - 10: count of positive Endoscopic Ultrasound(EUS) features: Parenchymal Features - Only Body and Tail Calcification (>3 hyperechoic foci >2 mm length & width with shadowing) Lobularity (>3 well-circumscribed, >5mm structures) Hyperechoic stranding (>3 hyperechoic lines >3mm in length, seen in > 2 different directions with respect to the imaged plane Parenchymal Features - Head, Body and Tail Cyst (>2 mm diameter anechoic round or oval structure) Hyperechoic foci (>3 reflectors, >3 mm long & wide, no shadowing) Ductal Features - Only Body and Tail Side Branch Dilation (>3 tubular, anechoic, >1 mm structures,Main pancreatic duct (MPD) connects) Irregular MPD contour (uneven and ectatic in its course) Hyperechoic MPD margin (hyperechoic in >50% of MPD) Dilation MPD (>3.5 mm body, >1.5 mm tail*) Ductal Features - Head, Body and Tail MPD calculi (hyperechoic foci with shadowing contained within MPD)
Quality of Life
The SF36 (Short Form with 36 questions) QoL scoring system has 36 questions, comprising two main dimensions (Physical Health and Mental Health), further divided by 8 independent scales (Physical functioning, Role-Physical, Bodily pain, General Health, Vitality, Social Functioning, Role-Emotional and Mental Health). The scales for general health and mental health overlap components of both the two main dimensions (Physical Health and Mental Health). The scales, including the total score and dimensions are scored as a number between 0 and 100, where 0 represents lower limits of functioning and 100 is best functioning possible. Data reported is the average total score.
Number and Percentage of Participants With Steatorrhea
Participants were counted as having steatorrhea if they had either a) positive qualitative fecal fat; or b) 72 hour quantitative fecal fat result with >7g fat in stool in 24hours
Pain
Pain is reported as the mean of four Visual analogue scales, ranging from 0 points (no pain) to 100 points (severe pain) What is your pain right now? What is your typical or average pain in the last 12 weeks? What is your pain level at its best in the last 12 weeks (how close to "0" does your pain get at its best)? What is your pain level at its worst in the last 12 weeks (how close to "0" does your pain get at its worst)?
Body Mass Index (BMI)
standard BMI defined as mass in kilograms divided by height in meters squared
Hospitalizations
Mean number of hospitalizations within the prior 12 weeks
Missed Work
Mean days of missed work reported by participants in response to question asking about missed work since the last visit (12 weeks)
Insulin Sensitivity (%S)
Homeostasis model assessment (HOMA 2) values generated using calculator at https://www.dtu.ox.ac.uk/homacalculator/;

Full Information

First Posted
October 29, 2008
Last Updated
December 11, 2017
Sponsor
University of Michigan
Collaborators
National Institute on Alcohol Abuse and Alcoholism (NIAAA), Takeda Pharmaceuticals North America, Inc.
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1. Study Identification

Unique Protocol Identification Number
NCT00782795
Brief Title
Chronic Pancreatitis. Effect of Pioglitazone on Endocrine Function, Exocrine Function & Structure, Pain & Life Quality
Official Title
Phase II Study of Chronic Pancreatitis and the Effect of Pioglitazone on Endocrine Function, Exocrine Function & Structure, Pain & Life Quality
Study Type
Interventional

2. Study Status

Record Verification Date
December 2017
Overall Recruitment Status
Completed
Study Start Date
November 2008 (undefined)
Primary Completion Date
December 2013 (Actual)
Study Completion Date
December 2013 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Michigan
Collaborators
National Institute on Alcohol Abuse and Alcoholism (NIAAA), Takeda Pharmaceuticals North America, Inc.

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The purpose of this study is to determine if study drug (Pioglitazone) treatment will improve pre-diabetes (insulin resistance) or ealy diabetes and improve clinical symptoms (pain) or laboratory evidence of chronic pancreatitis. The goal of the investigators is to gather information from this study to help gain understanding of a potential therapy for chronic pancreatitis.
Detailed Description
The pancreas is a digestive organ that secretes insulin (and other hormones) into the blood for regulating blood sugar (glucose) and digestive enzymes into the intestine for digesting and absorbing nutrients consumed in meals. Chronic pancreatitis is a progressive clinical disease of the pancreas, associated with swelling (inflammation), scarring (fibrosis) and loss of normal functioning tissue. Patients develop diabetes mellitus (elevated blood sugar), malabsorption of nutrients, weight loss and pain. Presently chronic pancreatitis is considered an irreversible condition because the mechanisms responsible for chronic pancreatitis are poorly understood and no therapy is proven. However, recent studies provide important clues that oral medications (Thiazolidinediones) used to treat diabetes mellitus might improve or reverse features of chronic pancreatitis, including elevated sugar or diabetes, reduced secretion of digestive enzymes, and pancreatic swelling and scarring. Note: Takeda Pharmaceuticals North America (TPNA) provided pioglitazone and placebo pills with identically appearance until June 28, 2010, approximately the middle of the study.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Chronic Pancreatitis, Insulin Resistance, Normal or Mildly Abnormal Stool Fat Levels
Keywords
Chronic pancreatitis, Insulin resistance

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
64 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Pioglitazone
Arm Type
Active Comparator
Arm Description
30 mg pioglitazone (Actos) tablet taken once daily for 48 weeks.
Arm Title
sugar pill (placebo)
Arm Type
Placebo Comparator
Arm Description
1 sugar pill (placebo) taken once daily for 48 weeks.
Intervention Type
Drug
Intervention Name(s)
Pioglitazone
Other Intervention Name(s)
Actos
Intervention Description
Participants randomized to pioglitazone receive 30 mg taken once daily for 48 weeks.
Intervention Type
Drug
Intervention Name(s)
Placebo
Primary Outcome Measure Information:
Title
Glucose Tolerance at 24 Weeks
Description
Normal = normal plasma glucose and normal glucose tolerance (OGTT). Impaired category includes all non-diabetic participants with either a) Impaired fasting glucose = fasting plasma glucose >110 mg/dl and <126 mg/dl; or b) Impaired glucose intolerance = 2-hour plasma glucose (OGTT) >140 mg/dl and <200 mg/dl. Diabetes = fasting plasma glucose >126 mg/dl 2-hour (OGTT) plasma glucose >200 mg/dl.
Time Frame
24 weeks
Title
Glucose Tolerance at 48 Weeks
Description
Normal = normal plasma glucose and normal glucose tolerance (OGTT). Impaired category includes all non-diabetic participants with either a) Impaired fasting glucose = fasting plasma glucose >110 mg/dl and <126 mg/dl; or b) Impaired glucose intolerance = 2-hour plasma glucose (OGTT) >140 mg/dl and <200 mg/dl. Diabetes = fasting plasma glucose >126 mg/dl 2-hour (OGTT) plasma glucose >200 mg/dl.
Time Frame
48 weeks
Title
Insulin Sensitivity Index for Glycemia at 24 Weeks
Description
Insulin Sensitivity = Index for Glycemia (ISI gly) = 2 / ([INSp x GLYp] + 1). GLYp = Glycemic 0-2 hr area = sum of normalized (based on institutional values) 0 & 2 hr glucose. INSp = Insulinemic 0-2 hr area = sum of normalized (based on institutional values) 0 & 2 hr insulin.
Time Frame
24 weeks
Title
Insulin Sensitivity Index for Glycemia at 48 Weeks.
Description
Insulin Sensitivity = Index for Glycemia (ISI gly) = 2 / ([INSp x GLYp] + 1). GLYp = Glycemic 0-2 hr area = sum of normalized (based on institutional values) 0 & 2 hr glucose. INSp = Insulinemic 0-2 hr area = sum of normalized (based on institutional values) 0 & 2 hr insulin.
Time Frame
48 weeks
Secondary Outcome Measure Information:
Title
Beta-cell Function
Description
Homeostasis model assessment (HOMA 2) values generated using calculator at https://www.dtu.ox.ac.uk/homacalculator/
Time Frame
24, 48 weeks
Title
Insulin Resistance at 24 and 48 Weeks
Description
Homeostasis model assessment (HOMA 2) values generated using calculator at https://www.dtu.ox.ac.uk/homacalculator/
Time Frame
24, 48 weeks
Title
Pancreas Ultrasound Appearance
Description
Mean score on a scale of 0 - 10: count of positive Endoscopic Ultrasound(EUS) features: Parenchymal Features - Only Body and Tail Calcification (>3 hyperechoic foci >2 mm length & width with shadowing) Lobularity (>3 well-circumscribed, >5mm structures) Hyperechoic stranding (>3 hyperechoic lines >3mm in length, seen in > 2 different directions with respect to the imaged plane Parenchymal Features - Head, Body and Tail Cyst (>2 mm diameter anechoic round or oval structure) Hyperechoic foci (>3 reflectors, >3 mm long & wide, no shadowing) Ductal Features - Only Body and Tail Side Branch Dilation (>3 tubular, anechoic, >1 mm structures,Main pancreatic duct (MPD) connects) Irregular MPD contour (uneven and ectatic in its course) Hyperechoic MPD margin (hyperechoic in >50% of MPD) Dilation MPD (>3.5 mm body, >1.5 mm tail*) Ductal Features - Head, Body and Tail MPD calculi (hyperechoic foci with shadowing contained within MPD)
Time Frame
48 weeks
Title
Quality of Life
Description
The SF36 (Short Form with 36 questions) QoL scoring system has 36 questions, comprising two main dimensions (Physical Health and Mental Health), further divided by 8 independent scales (Physical functioning, Role-Physical, Bodily pain, General Health, Vitality, Social Functioning, Role-Emotional and Mental Health). The scales for general health and mental health overlap components of both the two main dimensions (Physical Health and Mental Health). The scales, including the total score and dimensions are scored as a number between 0 and 100, where 0 represents lower limits of functioning and 100 is best functioning possible. Data reported is the average total score.
Time Frame
24, 48 weeks
Title
Number and Percentage of Participants With Steatorrhea
Description
Participants were counted as having steatorrhea if they had either a) positive qualitative fecal fat; or b) 72 hour quantitative fecal fat result with >7g fat in stool in 24hours
Time Frame
48 weeks
Title
Pain
Description
Pain is reported as the mean of four Visual analogue scales, ranging from 0 points (no pain) to 100 points (severe pain) What is your pain right now? What is your typical or average pain in the last 12 weeks? What is your pain level at its best in the last 12 weeks (how close to "0" does your pain get at its best)? What is your pain level at its worst in the last 12 weeks (how close to "0" does your pain get at its worst)?
Time Frame
12, 24, 36, 48 and 60 weeks
Title
Body Mass Index (BMI)
Description
standard BMI defined as mass in kilograms divided by height in meters squared
Time Frame
12, 24, 36, 48 and 60 weeks
Title
Hospitalizations
Description
Mean number of hospitalizations within the prior 12 weeks
Time Frame
12, 24, 36, 48 and 60 weeks
Title
Missed Work
Description
Mean days of missed work reported by participants in response to question asking about missed work since the last visit (12 weeks)
Time Frame
12, 24, 36, 48, 60 weeks
Title
Insulin Sensitivity (%S)
Description
Homeostasis model assessment (HOMA 2) values generated using calculator at https://www.dtu.ox.ac.uk/homacalculator/;
Time Frame
24 and 48 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Insulin resistance or mild diabetes mellitus Symptoms of abdominal pain Xray test showing damage to the pancreas Normal or mildly abnormal stool fat levels Exclusion Criteria: Mentally disabled patients Women who are planning pregnancy, pregnant or lactating/nursing Chronic pancreatitis is due to other specific conditions Autosomal dominant pancreatitis Classic cystic fibrosis with lung involvement Autoimmune pancreatitis Pancreatic cancer Biliary obstruction (non-pancreatic cause) Abdominal trauma Hypercalcemia Hypertriglyceridemia Surgical resection of the head of the pancreas Alcohol consumption within prior 2 months Specific medical conditions Gastric surgery Celiac sprue Crohns disease Heart failure Kidney failure Cirrhosis or liver disease Osteoporosis Blood clotting disorder Visual problems Low albumin Low BMI Specific medications *Diabetes drug treatment is allowed except for short-acting insulin, long-acting insule more than 15 units daily, pioglitazone, rosiglitazone, orlistat, acarbose, miglitol or voglibose.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Matthew DiMagno, M.D.
Organizational Affiliation
University of Michigan
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Michigan Health System
City
Ann Arbor
State/Province
Michigan
ZIP/Postal Code
48109
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No

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Chronic Pancreatitis. Effect of Pioglitazone on Endocrine Function, Exocrine Function & Structure, Pain & Life Quality

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