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Peripheral Artery Occlusive Diseases (PAOD) Study - Clinical Assessment

Primary Purpose

Peripheral Artery Disease

Status
Withdrawn
Phase
Phase 2
Locations
Germany
Study Type
Interventional
Intervention
high dose flavanoids
low dose flavanoids
Sponsored by
RWTH Aachen University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Peripheral Artery Disease focused on measuring PAOD, diabetis, vascular function, in diabetics with PAOD

Eligibility Criteria

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

Inclusion Criteria:

  1. Diabetes mellitus type 2 defined by the criteria of the American Diabetes Association

    • Fasted plasma glucose greater than 126 mg/dL
    • Plasma glucose levels greater than 200 mg/dL 2 hours after OGT
    • Casual plasma glucose greater than 200 mg/dL combined with diabetic symptoms.
  2. Endothelial dysfunction defined by FMD <4%
  3. No changes of medication for 2 months
  4. Significant PAOD (level IIb, III)

Exclusion Criteria:

  1. Ejection fraction <30%
  2. Malignoms
  3. Terminal renal failure with hemodialysis
  4. Relevant cardiac arrhythmias
  5. Acute inflammation defined as CRP >0,5 mg/dl
  6. PAOD (level IV)

Sites / Locations

  • Heinrich-Heine-University, Düsseldorf

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Experimental

Arm Label

1

2

Arm Description

Treatement with low dose flavanoids over 60 days

Treatment with high dose flavanoids over 60 days

Outcomes

Primary Outcome Measures

Vascular function

Secondary Outcome Measures

pain free walking distance

Full Information

First Posted
October 10, 2008
Last Updated
September 22, 2015
Sponsor
RWTH Aachen University
Collaborators
Heinrich-Heine University, Duesseldorf
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1. Study Identification

Unique Protocol Identification Number
NCT00771797
Brief Title
Peripheral Artery Occlusive Diseases (PAOD) Study - Clinical Assessment
Official Title
Clinical Study to Assess the Clinical Efficacy of Flavanol-rich Cocoa on Vascular Function in Diabetic Patients With PAOD
Study Type
Interventional

2. Study Status

Record Verification Date
September 2015
Overall Recruitment Status
Withdrawn
Why Stopped
investigator took study to university hospital duesseldorf
Study Start Date
October 2008 (undefined)
Primary Completion Date
December 2009 (Anticipated)
Study Completion Date
December 2009 (Anticipated)

3. Sponsor/Collaborators

Name of the Sponsor
RWTH Aachen University
Collaborators
Heinrich-Heine University, Duesseldorf

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
To assess the clinical efficacy and to simultaneously explore the underlying molecular mechanisms of the beneficial effects of flavanol-rich cocoa on vascular function diabetic patients with peripheral artery occlusive diseases (PAOD) of the lower extremities will be investigated.
Detailed Description
50 Type 2 diabetics according to the criteria of the American Diabetes Association suffering from PAOD with a pain free walking distance less than 200 m will be enrolled. In a randomized controlled parallel group study the before established novel 5-level approach of vascular diagnostics will be realised. In order to test the hypothesis, whether cocoa rich in flavanols improves vascular function of diabetic PAOD subjects will regularly intake flavanol rich cocoa (group 1: 975 mg/d, n=50 versus group 2: 90 mg/d, n=50) over a period of two months. Clinical endpoints are the Ankle-Brachial-Index, measured by Doppler ultrasound and the pain-free walking distance determined by a treadmill ergometer. All parameters of vascular diagnostic (see 5-level approach above) will be determined before and two month after cocoa ingestion.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Peripheral Artery Disease
Keywords
PAOD, diabetis, vascular function, in diabetics with PAOD

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
0 (Actual)

8. Arms, Groups, and Interventions

Arm Title
1
Arm Type
Experimental
Arm Description
Treatement with low dose flavanoids over 60 days
Arm Title
2
Arm Type
Experimental
Arm Description
Treatment with high dose flavanoids over 60 days
Intervention Type
Dietary Supplement
Intervention Name(s)
high dose flavanoids
Intervention Description
flavanoid rich cocoa 2 times daily over 60 days
Intervention Type
Dietary Supplement
Intervention Name(s)
low dose flavanoids
Intervention Description
treatment with flavanoid-low cocoa two times daily over 60 days
Primary Outcome Measure Information:
Title
Vascular function
Time Frame
before treatment and after 30 and 60 days
Secondary Outcome Measure Information:
Title
pain free walking distance
Time Frame
before treatment and 30 and 60 days afterwards

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Diabetes mellitus type 2 defined by the criteria of the American Diabetes Association Fasted plasma glucose greater than 126 mg/dL Plasma glucose levels greater than 200 mg/dL 2 hours after OGT Casual plasma glucose greater than 200 mg/dL combined with diabetic symptoms. Endothelial dysfunction defined by FMD <4% No changes of medication for 2 months Significant PAOD (level IIb, III) Exclusion Criteria: Ejection fraction <30% Malignoms Terminal renal failure with hemodialysis Relevant cardiac arrhythmias Acute inflammation defined as CRP >0,5 mg/dl PAOD (level IV)
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Tienush Rassaf, MD
Organizational Affiliation
Clinic for Cardiology, University Düsseldorf
Official's Role
Principal Investigator
Facility Information:
Facility Name
Heinrich-Heine-University, Düsseldorf
City
Düsseldorf
ZIP/Postal Code
40225
Country
Germany

12. IPD Sharing Statement

Learn more about this trial

Peripheral Artery Occlusive Diseases (PAOD) Study - Clinical Assessment

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