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Effects of Fenofibrate on Endothelial Progenitor Cells in Diabetes

Primary Purpose

Diabetes, Diabetic Retinopathy

Status
Completed
Phase
Phase 4
Locations
Italy
Study Type
Interventional
Intervention
Fenofibrate 145 mg
Placebo
Sponsored by
University of Padova
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional basic science trial for Diabetes focused on measuring Stem cells, Regeneration, Angiogenesis, Prevention

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Type 1 or type 2 diabetes
  • Diabetic retinopathy
  • Age 18-70
  • Both sexes

Exclusion Criteria:

  • Age <18 or >70 at enrollment
  • Hereditary muscle disorders
  • Uncontrolled hypothyroidism
  • Elevated alcohol consumption
  • Renal failure
  • Hepatic failure
  • Allergy to fenofibrate or excipients
  • Acute / chronic pancreatitis
  • Pregnancy and lactation.

Sites / Locations

  • University Hospital of Padova, Diabetes Outpatient Clinic

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

Fenofibrate

Placebo

Arm Description

Fenofibrate 145 mg (Fulcrosupra) oral tablets daily for 12 weeks

Placebo oral tablets daily for 12 weeks

Outcomes

Primary Outcome Measures

Endothelial progenitor cells
Change in endothelial progenitor cell (EPC) levels in fenofibrate-treated vs placebo-treated patients over 12 weeks.
Circulating progenitor cells
Change in circulating progenitor cell (CPC) levels in fenofibrate-treated vs placebo-treated patients over 12 weeks.

Secondary Outcome Measures

Triglycerides
Change in Triglycerideslevels in fenofibrate-treated vs placebo-treated patients over 12 weeks.

Full Information

First Posted
August 19, 2013
Last Updated
December 17, 2019
Sponsor
University of Padova
Collaborators
Azienda Ospedaliera di Padova
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1. Study Identification

Unique Protocol Identification Number
NCT01927315
Brief Title
Effects of Fenofibrate on Endothelial Progenitor Cells in Diabetes
Official Title
Effects of Fenofibrate on Endothelial Progenitor Cell Levels in Diabetic Patients With Retinopathy. A Randomized Controlled Trial.
Study Type
Interventional

2. Study Status

Record Verification Date
December 2019
Overall Recruitment Status
Completed
Study Start Date
August 2013 (Actual)
Primary Completion Date
October 2019 (Actual)
Study Completion Date
December 2019 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Padova
Collaborators
Azienda Ospedaliera di Padova

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Long-standing diabetes is often complicated by retinopathy. The mechanisms that induce the development of diabetic retinopathy are incompletely understood and include alterations in bone marrow derived vasculogenic cells called "endothelial progenitor cells". Fenofibrate is a PPAR-alpha agonist used for the treatment of mixed dislipidemia and hypertriglyceridemia. In a trial conducted in type 2 diabetic patients, the drug fenofibrate has reduced retinopathy-related endpoints suggesting a direct effect of the drug on the mechanisms that drive the development of this complication. Herein, the investigators hypothesize that fenofibrate treatment can increase circulating EPC levels in diabetic patients with retinopathy, compared to placebo.
Detailed Description
Long-standing diabetes is often complicated by retinopathy. The mechanisms that induce the development of diabetic retinopathy are incompletely understood and include alterations in bone marrow derived vasculogenic cells called "endothelial progenitor cells". Fenofibrate is a PPAR-alpha agonist used for the treatment of mixed dislipidemia and hypertriglyceridemia. In addition to lowering triglyceride-rich lipoproteins, PPAR-alpha agonism with fenofibrate has several additional molecular benefit on the vessel wall, such as reduction of inflammation. In a trial conducted in type 2 diabetic patients, the drug fenofibrate has reduced retinopathy-related endpoints suggesting a direct effect of the drug on the mechanisms that drive the development of this complication. Preliminary data of ours on the effects of fenofibrate on cultured EPC show that this drug has the potential to improve EPC and, consequently, may benefit patients with retinopathy. Herein, the investigators hypothesize that fenofibrate treatment can increase circulating EPC levels in diabetic patients with retinopathy, compared to placebo.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Diabetes, Diabetic Retinopathy
Keywords
Stem cells, Regeneration, Angiogenesis, Prevention

7. Study Design

Primary Purpose
Basic Science
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
Participant
Masking Description
Single blind
Allocation
Randomized
Enrollment
41 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Fenofibrate
Arm Type
Experimental
Arm Description
Fenofibrate 145 mg (Fulcrosupra) oral tablets daily for 12 weeks
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Placebo oral tablets daily for 12 weeks
Intervention Type
Drug
Intervention Name(s)
Fenofibrate 145 mg
Other Intervention Name(s)
Fulcrosupra 145 mg
Intervention Description
Tablets of Fulcrosupra 145 mg to be taken at 8.00 am daily for 12 weeks.
Intervention Type
Drug
Intervention Name(s)
Placebo
Other Intervention Name(s)
Placebo control
Intervention Description
Oral Placebo tablets once daily
Primary Outcome Measure Information:
Title
Endothelial progenitor cells
Description
Change in endothelial progenitor cell (EPC) levels in fenofibrate-treated vs placebo-treated patients over 12 weeks.
Time Frame
12 weeks
Title
Circulating progenitor cells
Description
Change in circulating progenitor cell (CPC) levels in fenofibrate-treated vs placebo-treated patients over 12 weeks.
Time Frame
12 weeks
Secondary Outcome Measure Information:
Title
Triglycerides
Description
Change in Triglycerideslevels in fenofibrate-treated vs placebo-treated patients over 12 weeks.
Time Frame
12 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Type 1 or type 2 diabetes Diabetic retinopathy Age 18-70 Both sexes Exclusion Criteria: Age <18 or >70 at enrollment Hereditary muscle disorders Uncontrolled hypothyroidism Elevated alcohol consumption Renal failure Hepatic failure Allergy to fenofibrate or excipients Acute / chronic pancreatitis Pregnancy and lactation.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Gian Paolo Fadini, MD PhD
Organizational Affiliation
University of Padova
Official's Role
Principal Investigator
Facility Information:
Facility Name
University Hospital of Padova, Diabetes Outpatient Clinic
City
Padova
ZIP/Postal Code
35100
Country
Italy

12. IPD Sharing Statement

Citations:
PubMed Identifier
34368894
Citation
Bonora BM, Albiero M, Morieri ML, Cappellari R, Amendolagine FI, Mazzucato M, Zambon A, Iori E, Avogaro A, Fadini GP. Fenofibrate increases circulating haematopoietic stem cells in people with diabetic retinopathy: a randomised, placebo-controlled trial. Diabetologia. 2021 Oct;64(10):2334-2344. doi: 10.1007/s00125-021-05532-1. Epub 2021 Aug 9.
Results Reference
derived

Learn more about this trial

Effects of Fenofibrate on Endothelial Progenitor Cells in Diabetes

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