TTA in Treatment of Diabetes and Dyslipidemia (TODDY)
Primary Purpose
Type 2 Diabetes Mellitus, Dyslipidemia
Status
Completed
Phase
Phase 2
Locations
Norway
Study Type
Interventional
Intervention
Tetradecylthioacetic acid (TTA)
Sponsored by
About this trial
This is an interventional treatment trial for Type 2 Diabetes Mellitus
Eligibility Criteria
Inclusion Criteria:
- type 2 diabetes mellitus with HbA1c 8.0-12.0%,
- fasting S-triacylglycerol 2.0-10.0 mmol/L,
- body mass index 25-40 kg/m2 and/or waist/hip ratio > 0.90.
Exclusion Criteria:
- fasting total cholesterol >10 mmol/L,
- blood pressure 170/110 mmHg
- other significant disease
- Use of any corticosteroid, anticoagulant or lipid-lowering drug 2 weeks prior to inclusion.
Sites / Locations
- Haukeland University Hospital
Arms of the Study
Arm 1
Arm Type
Active Comparator
Arm Label
Single group
Arm Description
Single group all treated similarly, outcome evaluated as changes within individuals during intervention
Outcomes
Primary Outcome Measures
Plasma lipids
Secondary Outcome Measures
Plasma glucose
Safety blood parameters
Full Information
NCT ID
NCT00605787
First Posted
January 17, 2008
Last Updated
January 17, 2008
Sponsor
Haukeland University Hospital
Collaborators
University of Bergen
1. Study Identification
Unique Protocol Identification Number
NCT00605787
Brief Title
TTA in Treatment of Diabetes and Dyslipidemia
Acronym
TODDY
Official Title
TTA in Treatment of Diabetes and Dyslipidemia
Study Type
Interventional
2. Study Status
Record Verification Date
January 2008
Overall Recruitment Status
Completed
Study Start Date
January 2002 (undefined)
Primary Completion Date
June 2003 (Actual)
Study Completion Date
December 2007 (Actual)
3. Sponsor/Collaborators
Name of the Sponsor
Haukeland University Hospital
Collaborators
University of Bergen
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
The aim of the study is to evaluate the short-term effects of tetradecylthioacetic acid (TTA) on plasma lipids and glucose in male patients with type 2 diabetes mellitus and dyslipidemia
Detailed Description
The tight linkage of obesity, insulin resistance (and frank diabetes), dyslipidemia, and hypertension has been widely observed and has been named syndrome X, or the metabolic syndrome. For many years metformin has been the only drug in clinical use with effects on insulin resistance. Recently, agonists of the peroxisome proliferator-activated receptors (PPARs) have been introduced in the treatment of type 2 diabetes. The different PPARs seem to be activated by a wide range of lipids and lipid mediators, including fatty acids. 2-tetradecylthioacetic acid (TTA) is a modified fatty acid with high affinity for the PPARgamma receptor. In animal models of obesity-related insulin resistance (obese Zucker rats and dietary manipulated Wistar rats), TTA has an insulin sensitizing effect by enhancing the insulin mediated uptake of glucose in peripheral tissues. TTA treatment promotes fatty acid catabolism in experimental animals and this could casually be linked to the improved glucose tolerance.
The protocol for the present study describes a safety assessment and therapeutic exploratory evaluation of TTA in a small subset of male type 2 diabetes patients for 4 weeks. The primary safety parameters will include general physical observational parameters, liver function test and hematological parameters. To goal is to assess the efficacy of TTA on selected metabolic parameters including fasting blood glucose and insulin, fasting plasma lipids, antioxidant status, and fibrinolytic parameters, weight, BMI and blood pressure.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Type 2 Diabetes Mellitus, Dyslipidemia
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
16 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Single group
Arm Type
Active Comparator
Arm Description
Single group all treated similarly, outcome evaluated as changes within individuals during intervention
Intervention Type
Drug
Intervention Name(s)
Tetradecylthioacetic acid (TTA)
Intervention Description
1000mg capsules once daily for 28 days
Primary Outcome Measure Information:
Title
Plasma lipids
Time Frame
-28 days, baseline, 14 and 28 days of TTA
Secondary Outcome Measure Information:
Title
Plasma glucose
Time Frame
-28 days, baseline, 14 and 28 days of TTA
Title
Safety blood parameters
Time Frame
-28 days, baseline, 14 and 28 days of TTA
10. Eligibility
Sex
Male
Minimum Age & Unit of Time
30 Years
Maximum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
type 2 diabetes mellitus with HbA1c 8.0-12.0%,
fasting S-triacylglycerol 2.0-10.0 mmol/L,
body mass index 25-40 kg/m2 and/or waist/hip ratio > 0.90.
Exclusion Criteria:
fasting total cholesterol >10 mmol/L,
blood pressure 170/110 mmHg
other significant disease
Use of any corticosteroid, anticoagulant or lipid-lowering drug 2 weeks prior to inclusion.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Eystein S Husebye, MD, PhD
Organizational Affiliation
Haukeland University Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Haukeland University Hospital
City
Bergen
ZIP/Postal Code
5021
Country
Norway
12. IPD Sharing Statement
Citations:
PubMed Identifier
19267708
Citation
Lovas K, Rost TH, Skorve J, Ulvik RJ, Gudbrandsen OA, Bohov P, Wensaas AJ, Rustan AC, Berge RK, Husebye ES. Tetradecylthioacetic acid attenuates dyslipidaemia in male patients with type 2 diabetes mellitus, possibly by dual PPAR-alpha/delta activation and increased mitochondrial fatty acid oxidation. Diabetes Obes Metab. 2009 Apr;11(4):304-14. doi: 10.1111/j.1463-1326.2008.00958.x.
Results Reference
derived
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TTA in Treatment of Diabetes and Dyslipidemia
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