Ischemic Injury and Ischemic Preconditioning in Diabetes

NCT00184821 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 20

Last updated 2007-04-05

No results posted yet for this study

Summary

In this proof-of-concept study, forearm vulnerability to ischemic exercise is studied in patients with type 1 diabetes mellitus with and without prior ischemic preconditioning (short period of ischemia that protects against subsequent ischemic exercise). Annexin A5 scintigraphy is used to quantify subtle signs of mild and reversible forearm injury that results from ischemic exercise.

The following hypotheses are tested:

1. Patients with type 1 diabetes are not more vulnerable to ischemic injury as compared with previously studied healthy volunteers.
2. Ischemic preconidtioning is still present in patients with type 1 diabetes. Depending on the validity of hypothesis 2, the effect of short pharmacological interventions are studied on vulnerability to forearm ischemia/reperfusion injury in the absence or presence of local forearm ischemic preconditioning.

Conditions

  • Diabetes Mellitus, Insulin-Dependent
  • Ischemia-Reperfusion Injury

Interventions

PROCEDURE

Ischemic preconditioning

PROCEDURE

Forearm ischemic exercise

PROCEDURE

Annexin A5 scintigraphy

DRUG

Diazoxide

DRUG

glibenclamide

DRUG

adenosine

Sponsors & Collaborators

  • Dutch Diabetes Fund

    collaborator UNKNOWN
  • Radboud University Medical Center

    lead OTHER

Principal Investigators

  • Richard Engbersen, MD · Radboud University Nijmegen Medical Centre; department of Pharmacology-Toxicology

  • Gerard Rongen, MD, PhD · Radboud University Nijmegen Medical Centre; Department of Pharmacology-Toxicology

  • Wim Oyen, MD, PhD · Radboud University Nijmegen Medical Centre; Department of Nuclear Medicine

  • Marc Mol, MD, PhD · Canisius Wilhelmina Ziekenhuis Nijmegen; Department of Internal Medicine

  • Paul Smits, MD, PhD · Radboud University Nijmegen Medical Centre; Department of Pharmacology-Toxicology

  • B. Bravenboer, MD, PhD · Catharina Hospital Eindhoven, Dept. of Internal Medicine

Eligibility

Min Age
18 Years
Max Age
50 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2004-06-30
Completion
2005-05-31

Countries

  • Netherlands

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00184821 on ClinicalTrials.gov