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Correlation of Flicker Induced and Flow Mediated Vasodilatation in Patients With Endothelial Dysfunction and Healthy Volunteers.

Primary Purpose

Diabetes Mellitus, Type 1, Hypertension, Hypercholesterolemia

Status
Completed
Phase
Not Applicable
Locations
Austria
Study Type
Interventional
Intervention
Forearm blood flow measurement, Flow mediated dilation (FMD)
Zeiss Retinal Vessel Analyzer (RVA), Stimulation with Flicker-light
Sponsored by
Medical University of Vienna
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Diabetes Mellitus, Type 1 focused on measuring Flicker induced vasodilatation, Flow mediated vasodilatation, Forearm blood flow, Retinal vessel diameter, Endothelial dysfunction

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

Patients with diabetic retinopathy:

  • Men and women aged > 18 years.
  • Normal findings in the medical history unless the investigator considers an abnormality to be clinically irrelevant.
  • Inclusion criteria of patients are insulin dependent diabetes mellitus (IDDM) with non or mild non-proliferative diabetic retinopathy. Patients with no signs of diabetic retinopathy (level 1) or patients with one or more microaneurysms (level 2) will be included. Level of diabetic retinopathy will be assessed according to the criteria defined in the AREDS-study.(1991)
  • serum cholesterol < 250 mg/dl (treated or untreated)

Patients with mild hypertension and/or hypercholesterinemia:

  • Men and women aged > 18 years.
  • mild essential hypertension defined as a blood pressure meeting the criterion of hypertension grade 1 of the World Health Organisation blood pressure classification
  • systolic blood pressure between 140 and 159 mmHg and diastolic blood pressure between 90 and 99 mmHg and/or
  • serum cholesterol > 250 mg/dl
  • blood pressure will be measured at two different occasion in a sitting positions

Healthy subjects:

  • Men and women aged > 18 years.
  • Normal findings in the medical history unless the investigator considers an abnormality to be clinically irrelevant
  • normal ocular findings
  • serum cholesterol < 200 mg/dl
  • systolic blood pressure between 110mmHg and 140mmHg
  • diastolic blood pressure < 90 mmHg

Exclusion Criteria:

  • Abuse of alcoholic beverages, participation in a clinical trial in the 3 weeks preceding the study
  • Symptoms of a clinically relevant illness in the 3 weeks before the first study day
  • Blood donation during the previous 3 weeks
  • other ocular pathologies than diabetic retinopathy level 1 or 2
  • History or family history of epilepsy
  • Ametropy greater or equal than 3 dpt
  • systolic blood pressure < 100mmHg
  • diastolic blood pressure < 75mmHg
  • pregnant or lactating women

Sites / Locations

  • Department of Clinical Pharmacology, Medical University of Vienna

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Other

Other

Other

Arm Label

1

2

3

Arm Description

IDDM

Hypercholesterolemia and/or Hypertension

age/sex matched healthy control subjects

Outcomes

Primary Outcome Measures

Retinal vessel diameters (Retinal vessel analyzer)
Forearm Blood Flow

Secondary Outcome Measures

Full Information

First Posted
February 5, 2007
Last Updated
July 1, 2008
Sponsor
Medical University of Vienna
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1. Study Identification

Unique Protocol Identification Number
NCT00432029
Brief Title
Correlation of Flicker Induced and Flow Mediated Vasodilatation in Patients With Endothelial Dysfunction and Healthy Volunteers.
Official Title
Correlation of Flicker Induced and Flow Mediated Vasodilatation in Patients With Endothelial Dysfunction and Healthy Volunteers
Study Type
Interventional

2. Study Status

Record Verification Date
June 2008
Overall Recruitment Status
Completed
Study Start Date
December 2006 (undefined)
Primary Completion Date
December 2007 (Actual)
Study Completion Date
January 2008 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
Medical University of Vienna

4. Oversight

5. Study Description

Brief Summary
A couple of studies have shown that illuminating the eye with diffuse flickering light is accompanied by an increase of retinal vessel diameters, optic nerve head blood flow and retinal blood flow. We have recently used this visual stimulation technique as a new and powerful tool for the non-invasive investigation of vascular reactivity. Additionally, we could show that this response is diminished in patients with vascular pathologies and that the response is dependent on nitric oxide, indicating that flicker induced vasodilatation may reflect endothelial dysfunction and may be a new approach to test endothelial function in vivo. One of the most widely used method for the assessment of endothelial function is flow mediated dilatation (FMD). FMD has been shown to give a reliable estimate of vascular function in vivo. In the present study, we set out to compare the standard method for the evaluation of endothelial function, FMD, to flicker induced vasodilatation in the retina.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Diabetes Mellitus, Type 1, Hypertension, Hypercholesterolemia, Regional Blood Flow
Keywords
Flicker induced vasodilatation, Flow mediated vasodilatation, Forearm blood flow, Retinal vessel diameter, Endothelial dysfunction

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
80 (Actual)

8. Arms, Groups, and Interventions

Arm Title
1
Arm Type
Other
Arm Description
IDDM
Arm Title
2
Arm Type
Other
Arm Description
Hypercholesterolemia and/or Hypertension
Arm Title
3
Arm Type
Other
Arm Description
age/sex matched healthy control subjects
Intervention Type
Procedure
Intervention Name(s)
Forearm blood flow measurement, Flow mediated dilation (FMD)
Intervention Description
Forearm blood flow measurement: baseline 1 min, 3 min after inflation of cuff, 4 min after 0.8mg Nitroglycerin
Intervention Type
Device
Intervention Name(s)
Zeiss Retinal Vessel Analyzer (RVA), Stimulation with Flicker-light
Intervention Description
Stimulation with Flicker-light: 1 min, measurement without flickering light 4 min after 0.8 mg Nitroglycerin
Primary Outcome Measure Information:
Title
Retinal vessel diameters (Retinal vessel analyzer)
Time Frame
8 min
Title
Forearm Blood Flow
Time Frame
8 min

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Patients with diabetic retinopathy: Men and women aged > 18 years. Normal findings in the medical history unless the investigator considers an abnormality to be clinically irrelevant. Inclusion criteria of patients are insulin dependent diabetes mellitus (IDDM) with non or mild non-proliferative diabetic retinopathy. Patients with no signs of diabetic retinopathy (level 1) or patients with one or more microaneurysms (level 2) will be included. Level of diabetic retinopathy will be assessed according to the criteria defined in the AREDS-study.(1991) serum cholesterol < 250 mg/dl (treated or untreated) Patients with mild hypertension and/or hypercholesterinemia: Men and women aged > 18 years. mild essential hypertension defined as a blood pressure meeting the criterion of hypertension grade 1 of the World Health Organisation blood pressure classification systolic blood pressure between 140 and 159 mmHg and diastolic blood pressure between 90 and 99 mmHg and/or serum cholesterol > 250 mg/dl blood pressure will be measured at two different occasion in a sitting positions Healthy subjects: Men and women aged > 18 years. Normal findings in the medical history unless the investigator considers an abnormality to be clinically irrelevant normal ocular findings serum cholesterol < 200 mg/dl systolic blood pressure between 110mmHg and 140mmHg diastolic blood pressure < 90 mmHg Exclusion Criteria: Abuse of alcoholic beverages, participation in a clinical trial in the 3 weeks preceding the study Symptoms of a clinically relevant illness in the 3 weeks before the first study day Blood donation during the previous 3 weeks other ocular pathologies than diabetic retinopathy level 1 or 2 History or family history of epilepsy Ametropy greater or equal than 3 dpt systolic blood pressure < 100mmHg diastolic blood pressure < 75mmHg pregnant or lactating women
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Michael Wolzt, MD
Organizational Affiliation
Department of Clinical Pharmacology, Medical University of Vienna
Official's Role
Principal Investigator
Facility Information:
Facility Name
Department of Clinical Pharmacology, Medical University of Vienna
City
Vienna
ZIP/Postal Code
1090
Country
Austria

12. IPD Sharing Statement

Citations:
PubMed Identifier
19369238
Citation
Pemp B, Garhofer G, Weigert G, Karl K, Resch H, Wolzt M, Schmetterer L. Reduced retinal vessel response to flicker stimulation but not to exogenous nitric oxide in type 1 diabetes. Invest Ophthalmol Vis Sci. 2009 Sep;50(9):4029-32. doi: 10.1167/iovs.08-3260. Epub 2009 Apr 15.
Results Reference
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Correlation of Flicker Induced and Flow Mediated Vasodilatation in Patients With Endothelial Dysfunction and Healthy Volunteers.

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