Effects of Exercise Training and AGE-crosslink Breaker on Cardiovascular Structure and Function

NCT01417663 · Status: COMPLETED · Phase: PHASE2/PHASE3 · Type: INTERVENTIONAL · Enrollment: 48

Last updated 2013-09-09

No results posted yet for this study

Summary

Healthy but sedentary aging leads to increased morbidity and mortality of cardiovascular disease. This is partly due to the accumulation of Advanced Glycation Endproducts (AGEs) and the stiffening of the myocardium and arteries. New medication has been developed to break these AGE-crosslinks to improve cardiovascular compliance. The positive influence of regular physical activity is well known for cardiovascular disease and aging. Therefore, what is the most effective intervention, physical exercise and/or new medication AGE-crosslink breakers, in improving the cardiovascular and cerebrovascular compliance and improving the endothelial function in healthy sedentary elderly.

Conditions

Interventions

DRUG

Alt-711

Alt-711, also known as Alagebrium, an AGE-crosslink breaker, will be given twice daily 100mg

BEHAVIORAL

Physical exercise training

Exercise training will be given three times a week for 45 minutes per training session. The heart rate reserve will be slowly increased from 70% to 85%.

Sponsors & Collaborators

  • Dutch Heart Foundation

    collaborator OTHER
  • Synvista Therapeutics, Inc

    collaborator INDUSTRY
  • Radboud University Medical Center

    lead OTHER

Principal Investigators

  • Maria TE Hopman, MD, PhD · Radboud University Medical Center

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
QUADRUPLE
Model
FACTORIAL

Eligibility

Min Age
65 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2008-11-30
Primary Completion
2011-06-30
Completion
2011-06-30

Countries

  • Netherlands

Study Locations

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Entities

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 NCT01417663 on ClinicalTrials.gov