Trial record 16 of 94 for:    "ACDC"

Adiponectin and Circulating Progenitor Cells (CPC) Function

This study has been completed.
Sponsor:
Collaborator:
German Research Foundation
Information provided by:
University of Leipzig
ClinicalTrials.gov Identifier:
NCT01272674
First received: January 7, 2011
Last updated: March 11, 2011
Last verified: January 2011
  Purpose

Adiponectin and exercise training contribute to the maintenance of a normal vascular tone by influencing vascular NO bioavailability and concentration and function of endothelial progenitor cells. The molecular mechanisms are only partially understood. Therefore, aim of the present study is to elucidate the effects of Adiponectin on endothelial progenitor cell migration and the underlying signaling pathways. Furthermore, the impact of exercise training on adiponectin-mediated endothelial progenitor cell migration will be investigated.


Condition Intervention Phase
Coronary Artery Disease
Other: exercise training
Phase 1

Study Type: Interventional
Study Design: Allocation: Randomized
Endpoint Classification: Efficacy Study
Intervention Model: Parallel Assignment
Masking: Open Label
Primary Purpose: Basic Science
Official Title: Adiponectin Promotes the Migration of Circulating Progenitor Cells Through p38-mediated Induction of the CXCR4 Receptor

Resource links provided by NLM:


Further study details as provided by University of Leipzig:

Primary Outcome Measures:
  • migratory capacity of endothelial progenitor cells towards an SDF-1 gradient [ Time Frame: 4 weeks ] [ Designated as safety issue: No ]

Estimated Enrollment: 20
Study Start Date: January 2011
Study Completion Date: March 2011
Primary Completion Date: March 2011 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Active Comparator: exercise training
4 weeks of supervised physical exercise training
Other: exercise training
4 weeks supervised physical exercise training
No Intervention: control
sedentary lifestyle
Other: exercise training
4 weeks supervised physical exercise training
No Intervention: healthy control

  Eligibility

Ages Eligible for Study:   18 Years to 75 Years
Genders Eligible for Study:   Male
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

  • ≤ 75 years of age
  • stable coronary artery disease
  • preserved left ventricular function
  • physical work capacity of ≥ 50
  • successful elective percutaneous coronary intervention at study begin

Exclusion Criteria:

  • diabetes mellitus
  • hypercholesterolemia
  • untreated hypertension
  • smoking
  • myocardial infarction within the last 4 weeks
  • significant stenosis of the left main coronary artery
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT01272674

Locations
Germany
University of Leipzig, Heart Center
Leipzig, Germany, 04289
Sponsors and Collaborators
University of Leipzig
German Research Foundation
Investigators
Principal Investigator: Axel Linke, MD University of Leipzig
  More Information

No publications provided

Responsible Party: Axel Linke, MD, Heart Center Leipzig
ClinicalTrials.gov Identifier: NCT01272674     History of Changes
Other Study ID Numbers: adipo2008
Study First Received: January 7, 2011
Last Updated: March 11, 2011
Health Authority: Germany: Federal Institue for Drugs and Medicinal Devices

Additional relevant MeSH terms:
Coronary Artery Disease
Coronary Disease
Myocardial Ischemia
Arterial Occlusive Diseases
Arteriosclerosis
Cardiovascular Diseases
Heart Diseases
Vascular Diseases

ClinicalTrials.gov processed this record on October 21, 2014