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The DIAMOND Study: Distensibility Improvement And Remodeling in Diastolic Heart Failure
This study has been completed.
Study NCT00043836   Information provided by Synvista Therapeutics, Inc
First Received: August 14, 2002   Last Updated: September 1, 2009   History of Changes

August 14, 2002
September 1, 2009
July 2002
February 2003   (final data collection date for primary outcome measure)
 
 
Complete list of historical versions of study NCT00043836 on ClinicalTrials.gov Archive Site
 
 
 
The DIAMOND Study: Distensibility Improvement And Remodeling in Diastolic Heart Failure
A Pilot Study Of ALT-711 In Elderly Patients With Isolated Diastolic Heart Failure: The DIAMOND Study

The purpose of this study is to test the hypothesis that treatment with oral ALT-711 twice daily for 16 weeks will improve aortic distensibility, exercise tolerance, and quality of life in elderly patients with isolated diastolic heart failure (DHF), and that the improvements in exercise tolerance will correlate with the improvements in aortic distensibility.

 
Phase II
Interventional
Treatment, Non-Randomized, Open Label, Historical Control, Single Group Assignment, Safety/Efficacy Study
  • Heart Failure, Congestive
  • Dyspnea
  • Pulmonary Edema
Drug: ALT-711
 

*   Includes publications given by the data provider as well as publications identified by National Clinical Trials Identifier (NCT ID) in Medline.
 
Completed
20
October 2005
February 2003   (final data collection date for primary outcome measure)

Inclusion Criteria

  1. Men or women ≥ 60 years of age.
  2. Diagnosis of congestive heart failure with one or both of the following criteria: a Heart Failure Clinical Score ≥ 3 based on the NHANES-I criteria and/or a history of either acute pulmonary edema or the occurrence of 2 or more of the following with subsequent improvement with diuretic therapy and with no other identifiable cause: dyspnea on exertion, paroxysmal nocturnal dyspnea, orthopnea, systemic edema, exertional fatigue.
  3. Left ventricular ejection fraction ≥ 50% based on the baseline Doppler echocardiography test.
  4. Ability to provide written informed consent.
  5. Ability to comply with procedures specified in the study protocol.

Exclusion Criteria

  1. Valvular heart disease as the primary etiology of congestive heart failure.
  2. Significant change in cardiovascular medication(s) <3 weeks prior to the baseline visit.
  3. Uncontrolled hypertension.
  4. History of stroke, or any sequelae of a transient ischemic attack (TIA), reversible ischemic neurologic defect (RIND), or stroke, within the last 12 months prior to entry into the study.
  5. Cancer or other noncardiovascular conditions with life expectancy less than 2 years.
  6. Significant anemia defined as a hemoglobin <11 gm/dL.
  7. Significant renal insufficiency defined as a serum creatinine >2.5 mg/dL.
  8. Significant hepatic insufficiency defined as an SGPT (ALT) or SGOT (AST) >2.5 times the upper limit of normal.
  9. Psychiatric disease (including uncontrolled major psychoses, depression, dementia, or personality disorder) or any additional condition(s) which, in the investigator's opinion, would prohibit the patient from completing the study, or not be in the best interest of the patient.
  10. Presence or history of drug or alcohol abuse.
  11. Prior exposure to ALT-711 or use of any other investigational drugs within 30 days prior to screening.
  12. Known seropositivity for HIV or hepatitis C, or presence of hepatitis B surface antigen.
  13. Severe COPD requiring recurrent oral steroids, oxygen at home or more than one inhaler.
  14. Baseline echocardiogram demonstrating the presence of left ventricular ejection fraction <50%.
  15. Unstable or uncontrolled myocardial ischemia, with no wall abnormality.
  16. Screening Familiarization Exercise Test demonstrating the presence of any of the following findings: evidence of significant ischemia (consisting of ECG finding of > 1 mm flat ST depression confirmed with echocardiogram wall motion, or wall motion abnormality or decrease in global contractility on echocardiogram, or inability to continue exercising due to significant chest or leg pain or any reason other than exhaustion/fatigue/dyspnea, exercise SBP >240 mm Hg, DBP >110 mmHg, unstable hemodynamics or rhythm, or unwilling or unable to complete test adequately.
  17. Any contraindications to magnetic resonance imaging including but not limited to indwelling metal-containing prosthesis (orthopedic, valvular, other), pacemaker or defibrillator, history of welding occupation (ocular metal debris), or uncontrollable claustrophobia.
Both
60 Years and older
No
Contact information is only displayed when the study is recruiting subjects
United States
 
NCT00043836
 
ALT-711-0214
Synvista Therapeutics, Inc
 
Principal Investigator: Dalane W Kitzman, MD Associate Professor of Medicine and Cardiology, Wake Forest University Baptist Medical Center
Principal Investigator: Michael R Zile, MD Charles Ezra Daniel Professor of Medicine, Medical University of South Carolina
Synvista Therapeutics, Inc
August 2007

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP