Liraglutide and a Calorie Restricted Diet Augments Weight Loss and Decreases Risk of Type 2 Diabetes and CVD.
Primary Purpose
Pre-diabetes, Older Adults
Status
Completed
Phase
Phase 3
Locations
Study Type
Interventional
Intervention
liraglutide
Placebo
Sponsored by
About this trial
This is an interventional prevention trial for Pre-diabetes
Eligibility Criteria
Inclusion Criteria:
IFG, or IGT BMI 27.0-37.0 kg/m2
Exclusion Criteria:
DM, CAD, severe anemia, kidney or liver disease, hx of pancreatitis, gallstones, ETOH abuse, personnel or family history of medullary thyroid carcinoma or MEN-2
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm Type
Placebo Comparator
Active Comparator
Arm Label
placebo
liraglutide
Arm Description
Both groups receive dietary weight loss intervention In addition one group received liraglutide and one group received placebo
Both groups receive dietary weight loss intervention In addition one group received liraglutide and one group received placebo
Outcomes
Primary Outcome Measures
Change in Weight Reported at 14 Weeks
Change in weight with caloric restriction plus liraglutide vs. caloric restriction and placebo over 14 weeks.
Secondary Outcome Measures
Glucose-stimulated Insulin Secretion in Insulin AUC, Pmol/1x 4H
Absolute change in glucose-stimulated insulin secretion (GS-IS) associated with caloric restriction plus liraglutide vs. caloric restriction and placebo at 14 weeks
Insulin Resistance in the Liraglutide vs.Placebo Group After Calorie Restriction
Mean (+/- SD) change in insulin resistance associated with caloric restriction plus liraglutide vs. caloric restriction and placebo.
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT01784965
Brief Title
Liraglutide and a Calorie Restricted Diet Augments Weight Loss and Decreases Risk of Type 2 Diabetes and CVD.
Official Title
Addition of a Glucagon-like Peptide-1 to a Calorie Restricted Diet Augments Weight Loss and Decreases Risk of Type 2 Diabetes and Cardiovascular Disease.
Study Type
Interventional
2. Study Status
Record Verification Date
March 2017
Overall Recruitment Status
Completed
Study Start Date
December 2009 (undefined)
Primary Completion Date
December 2012 (Actual)
Study Completion Date
December 2012 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Stanford University
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
The goal of this study is to evaluate the hypothesis that the addition of liraglutide, a long-acting glucagon-like peptide 1 (GLP-1) analogue, to a calorie-restricted diet will lead to greater weight loss than will a calorie-restricted diet alone in subjects who are older (50 to 60 years of age), overweight/obese, and prediabetic. These individuals have been selected for study because they are at greatly increased risk to develop type 2 diabetes (2DM) and cardiovascular disease (CVD), and it is hypothesized that the addition of liraglutide to a calorie-restricted diet will significantly decrease risk of these adverse outcomes.
There is considerable evidence that GLP-I compounds, including liraglutide, improve glycemic control in patients with manifest 2DM. However, there is relatively little information as to the potential utility of these compounds in nondiabetic individual at greatly increased risk of 2DM and CVD. This research proposal is aimed at providing some of this information by quantifying the effects of liraglutide, a long-acting GLP-1 analogue, on weight loss, insulin secretion, insulin action, and multiple CVD risk factors in a very high risk group-older, overweight/obese, prediabetic individuals. Furthermore, by using specific methods, not surrogate estimates, and avoiding the confounding effects of glucotoxicity, it will be possible to gain new insights into the effects of GLP-1 on insulin secretion and insulin action.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Pre-diabetes, Older Adults
7. Study Design
Primary Purpose
Prevention
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
69 (Actual)
8. Arms, Groups, and Interventions
Arm Title
placebo
Arm Type
Placebo Comparator
Arm Description
Both groups receive dietary weight loss intervention In addition one group received liraglutide and one group received placebo
Arm Title
liraglutide
Arm Type
Active Comparator
Arm Description
Both groups receive dietary weight loss intervention In addition one group received liraglutide and one group received placebo
Intervention Type
Drug
Intervention Name(s)
liraglutide
Other Intervention Name(s)
Victoza
Intervention Description
Dosing begins at 0.6 mg subcutaneous injection and increases each week, to 1.2 mg and maximum dose of 1.8 mg.
Intervention Type
Drug
Intervention Name(s)
Placebo
Intervention Description
Double blinded will receive study pen with same dosing instructions starting at 0.6 mg, and each week increase to 1.2 mg and finally 1.8 mg at week three.
Primary Outcome Measure Information:
Title
Change in Weight Reported at 14 Weeks
Description
Change in weight with caloric restriction plus liraglutide vs. caloric restriction and placebo over 14 weeks.
Time Frame
Baseline and 14 weeks
Secondary Outcome Measure Information:
Title
Glucose-stimulated Insulin Secretion in Insulin AUC, Pmol/1x 4H
Description
Absolute change in glucose-stimulated insulin secretion (GS-IS) associated with caloric restriction plus liraglutide vs. caloric restriction and placebo at 14 weeks
Time Frame
Baseline, 14 weeks
Title
Insulin Resistance in the Liraglutide vs.Placebo Group After Calorie Restriction
Description
Mean (+/- SD) change in insulin resistance associated with caloric restriction plus liraglutide vs. caloric restriction and placebo.
Time Frame
Baseline, 14 weeks
10. Eligibility
Sex
All
Minimum Age & Unit of Time
40 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
IFG, or IGT BMI 27.0-37.0 kg/m2
Exclusion Criteria:
DM, CAD, severe anemia, kidney or liver disease, hx of pancreatitis, gallstones, ETOH abuse, personnel or family history of medullary thyroid carcinoma or MEN-2
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Gerald M Reaven, M.D.
Organizational Affiliation
Stanford University
Official's Role
Principal Investigator
12. IPD Sharing Statement
Plan to Share IPD
No
Citations:
PubMed Identifier
24326527
Citation
Kim SH, Liu A, Ariel D, Abbasi F, Lamendola C, Grove K, Tomasso V, Reaven G. Pancreatic beta cell function following liraglutide-augmented weight loss in individuals with prediabetes: analysis of a randomised, placebo-controlled study. Diabetologia. 2014 Mar;57(3):455-62. doi: 10.1007/s00125-013-3134-3. Epub 2013 Dec 11.
Results Reference
derived
PubMed Identifier
23835684
Citation
Kim SH, Abbasi F, Lamendola C, Liu A, Ariel D, Schaaf P, Grove K, Tomasso V, Ochoa H, Liu YV, Chen YD, Reaven G. Benefits of liraglutide treatment in overweight and obese older individuals with prediabetes. Diabetes Care. 2013 Oct;36(10):3276-82. doi: 10.2337/dc13-0354. Epub 2013 Jul 8.
Results Reference
derived
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Liraglutide and a Calorie Restricted Diet Augments Weight Loss and Decreases Risk of Type 2 Diabetes and CVD.
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