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The Metformin-FMD Trial (MetFMD)

Primary Purpose

Ischemia Reperfusion Injury, Endothelial Function

Status
Completed
Phase
Phase 4
Locations
Netherlands
Study Type
Interventional
Intervention
Metformin
Pretreatment with metformin in combination of infusion of caffeine.
No pretreatment with metformin in combination with infusion of caffeine
Sponsored by
Radboud University Medical Center
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Ischemia Reperfusion Injury

Eligibility Criteria

30 Years - 50 Years (Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Age 30-50 years
  • Written informed consent

Exclusion Criteria:

  • Smoking
  • Hypertension (in supine position: systolic BP > 140 mmHg, diastolic BP > 90 mmHg)
  • Hyperlipidaemia (fasting total cholesterol > 5.5 mmol/L or random > 6.5 mmol/L)
  • Diabetes Mellitus (fasting glucose > 7.0 mmol/L or random glucose > 11.0 mmol/L)
  • History of any cardiovascular disease
  • Concomitant use of medication
  • Renal dysfunction (MDRD < 60 ml/min)
  • Professional athletes

Sites / Locations

  • Radboud University Nijmegen Medical Centre

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Active Comparator

No Intervention

Active Comparator

Other

Arm Label

Pretreatment with metformin

No pretreatment.

Pretreatment with Metformin/caffeine

No metformin, only pretreatment with caffeine

Arm Description

Pretreatment with metformin 500 mg three times a day for 3 days.

no intervention

to study whether caffeine (4 mg/kg intravenously over 10 minutes) attenuates the protective effect of metformin (500 mg three times a day for 3 days) on FMD after ischemia/reperfusion

No pretreatment with metformin, FMD measurement after forearm ischemia/reperfusion and infusion of caffeine (4 mg/kg intravenously over 10 minutes).

Outcomes

Primary Outcome Measures

Metformin-FMD trial: The effect of pretreatment with metformin on FMD of the brachial artery after forearm ischemia and reperfusion.
Metformin-FMD trial: To study the effect of oral pretreatment with metformin (500 mg three times ad ay for 3 days) on flow mediated dilation of the brachial artery after 20 minutes of forearm ischemia and 20 minutes of reperfusion in healthy volunteers.
Control trial: the effect of caffeine on the protective effect of metformin on FMD after ischemia and reperfusion.
Control trial: when metformin displays a protective effect on endothelial function, we will conduct a second experiment to study whether caffeine, an adenosine receptor antagonist, attenuates the protective effect of metformin on flow mediated dilation after 20 minutes of ischemia and 20 minutes of reperfusion in healthy volunteers.

Secondary Outcome Measures

Full Information

First Posted
May 25, 2012
Last Updated
May 17, 2013
Sponsor
Radboud University Medical Center
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1. Study Identification

Unique Protocol Identification Number
NCT01610401
Brief Title
The Metformin-FMD Trial
Acronym
MetFMD
Official Title
Can Metformin Prevent Endothelial Ischemia and Reperfusion Injury? The Metformin-FMD Trial
Study Type
Interventional

2. Study Status

Record Verification Date
February 2012
Overall Recruitment Status
Completed
Study Start Date
May 2012 (undefined)
Primary Completion Date
January 2013 (Actual)
Study Completion Date
January 2013 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Radboud University Medical Center

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
In acute myocardial infarction early restoration of coronary blood flow is the most effective strategy to limit infarct-size. Paradoxically, reperfusion itself also aggravates myocardial injury and contributes to final infarct size, a process termed 'reperfusion injury'. Ischemia and reperfusion (IR)-induced endothelial dysfunction seems to play a pivotal role in this process, resulting in vasoconstriction and reduced blood flow to the already ischemic tissue. Recently, it has been shown that the glucose-lowering drug metformin is able to limit IR-injury in murine models of myocardial infarction, probably by increased formation of the endogenous nucleoside adenosine. In the current research proposal, the investigators aim to translate this finding to the human in vivo situation, using flow-mediated dilation (FMD) of the brachial artery as a well-validated model of (endothelial) IR-injury.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Ischemia Reperfusion Injury, Endothelial Function

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Crossover Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
26 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Pretreatment with metformin
Arm Type
Active Comparator
Arm Description
Pretreatment with metformin 500 mg three times a day for 3 days.
Arm Title
No pretreatment.
Arm Type
No Intervention
Arm Description
no intervention
Arm Title
Pretreatment with Metformin/caffeine
Arm Type
Active Comparator
Arm Description
to study whether caffeine (4 mg/kg intravenously over 10 minutes) attenuates the protective effect of metformin (500 mg three times a day for 3 days) on FMD after ischemia/reperfusion
Arm Title
No metformin, only pretreatment with caffeine
Arm Type
Other
Arm Description
No pretreatment with metformin, FMD measurement after forearm ischemia/reperfusion and infusion of caffeine (4 mg/kg intravenously over 10 minutes).
Intervention Type
Drug
Intervention Name(s)
Metformin
Intervention Description
metformin 500 mg three times a day, for 3 days
Intervention Type
Drug
Intervention Name(s)
Pretreatment with metformin in combination of infusion of caffeine.
Intervention Description
Pretreatment with metformin 500 mg three times a day for 3 days, in combination with pretreatment with caffeine (4 mg/kg intravenously over 10 minutes) prior to FMD measurement
Intervention Type
Drug
Intervention Name(s)
No pretreatment with metformin in combination with infusion of caffeine
Intervention Description
No pretreatment with metformin in combination with pretreatment with caffeine (4 mg/kg intravenously over 10 minutes).
Primary Outcome Measure Information:
Title
Metformin-FMD trial: The effect of pretreatment with metformin on FMD of the brachial artery after forearm ischemia and reperfusion.
Description
Metformin-FMD trial: To study the effect of oral pretreatment with metformin (500 mg three times ad ay for 3 days) on flow mediated dilation of the brachial artery after 20 minutes of forearm ischemia and 20 minutes of reperfusion in healthy volunteers.
Time Frame
approx. 6 months
Title
Control trial: the effect of caffeine on the protective effect of metformin on FMD after ischemia and reperfusion.
Description
Control trial: when metformin displays a protective effect on endothelial function, we will conduct a second experiment to study whether caffeine, an adenosine receptor antagonist, attenuates the protective effect of metformin on flow mediated dilation after 20 minutes of ischemia and 20 minutes of reperfusion in healthy volunteers.
Time Frame
approx. 6 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
30 Years
Maximum Age & Unit of Time
50 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Age 30-50 years Written informed consent Exclusion Criteria: Smoking Hypertension (in supine position: systolic BP > 140 mmHg, diastolic BP > 90 mmHg) Hyperlipidaemia (fasting total cholesterol > 5.5 mmol/L or random > 6.5 mmol/L) Diabetes Mellitus (fasting glucose > 7.0 mmol/L or random glucose > 11.0 mmol/L) History of any cardiovascular disease Concomitant use of medication Renal dysfunction (MDRD < 60 ml/min) Professional athletes
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
N. Riksen, MD, PhD
Organizational Affiliation
Radboud University Medical Center
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
G.A. Rongen, M.D.
Organizational Affiliation
Radboud University Medical Center
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
D.H. Thijssen, PhD
Organizational Affiliation
Radboud University Medical Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
Radboud University Nijmegen Medical Centre
City
Nijmegen
State/Province
Gelderland
ZIP/Postal Code
6500 HB
Country
Netherlands

12. IPD Sharing Statement

Citations:
PubMed Identifier
24755906
Citation
El Messaoudi S, Schreuder TH, Kengen RD, Rongen GA, van den Broek PH, Thijssen DH, Riksen NP. Impact of metformin on endothelial ischemia-reperfusion injury in humans in vivo: a prospective randomized open, blinded-endpoint study. PLoS One. 2014 Apr 22;9(4):e96062. doi: 10.1371/journal.pone.0096062. eCollection 2014.
Results Reference
derived

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The Metformin-FMD Trial

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