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The DIAMOND Study: Distensibility Improvement And Remodeling in Diastolic Heart Failure

Primary Purpose

Heart Failure, Congestive, Dyspnea, Pulmonary Edema

Status
Completed
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
ALT-711
Sponsored by
Synvista Therapeutics, Inc
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Heart Failure, Congestive focused on measuring ejection fraction, exercise tolerance, heart failure, congestive, quality of life

Eligibility Criteria

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

Inclusion Criteria Men or women ≥ 60 years of age. 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. Left ventricular ejection fraction ≥ 50% based on the baseline Doppler echocardiography test. Ability to provide written informed consent. Ability to comply with procedures specified in the study protocol. Exclusion Criteria Valvular heart disease as the primary etiology of congestive heart failure. Significant change in cardiovascular medication(s) <3 weeks prior to the baseline visit. Uncontrolled hypertension. 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. Cancer or other noncardiovascular conditions with life expectancy less than 2 years. Significant anemia defined as a hemoglobin <11 gm/dL. Significant renal insufficiency defined as a serum creatinine >2.5 mg/dL. Significant hepatic insufficiency defined as an SGPT (ALT) or SGOT (AST) >2.5 times the upper limit of normal. 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. Presence or history of drug or alcohol abuse. Prior exposure to ALT-711 or use of any other investigational drugs within 30 days prior to screening. Known seropositivity for HIV or hepatitis C, or presence of hepatitis B surface antigen. Severe COPD requiring recurrent oral steroids, oxygen at home or more than one inhaler. Baseline echocardiogram demonstrating the presence of left ventricular ejection fraction <50%. Unstable or uncontrolled myocardial ischemia, with no wall abnormality. 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. 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.

Sites / Locations

  • Wake Forest University Baptist Medical Center, Department of Cardiology
  • Medical University of South Carolina and Ralph H. Johnson VA Medical Center

Outcomes

Primary Outcome Measures

Secondary Outcome Measures

Full Information

First Posted
August 14, 2002
Last Updated
September 1, 2009
Sponsor
Synvista Therapeutics, Inc
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1. Study Identification

Unique Protocol Identification Number
NCT00043836
Brief Title
The DIAMOND Study: Distensibility Improvement And Remodeling in Diastolic Heart Failure
Official Title
A Pilot Study Of ALT-711 In Elderly Patients With Isolated Diastolic Heart Failure: The DIAMOND Study
Study Type
Interventional

2. Study Status

Record Verification Date
August 2007
Overall Recruitment Status
Completed
Study Start Date
July 2002 (undefined)
Primary Completion Date
February 2003 (Actual)
Study Completion Date
October 2005 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
Synvista Therapeutics, Inc

4. Oversight

5. Study Description

Brief Summary
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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Heart Failure, Congestive, Dyspnea, Pulmonary Edema
Keywords
ejection fraction, exercise tolerance, heart failure, congestive, quality of life

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
20 (false)

8. Arms, Groups, and Interventions

Intervention Type
Drug
Intervention Name(s)
ALT-711

10. Eligibility

Sex
All
Minimum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria Men or women ≥ 60 years of age. 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. Left ventricular ejection fraction ≥ 50% based on the baseline Doppler echocardiography test. Ability to provide written informed consent. Ability to comply with procedures specified in the study protocol. Exclusion Criteria Valvular heart disease as the primary etiology of congestive heart failure. Significant change in cardiovascular medication(s) <3 weeks prior to the baseline visit. Uncontrolled hypertension. 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. Cancer or other noncardiovascular conditions with life expectancy less than 2 years. Significant anemia defined as a hemoglobin <11 gm/dL. Significant renal insufficiency defined as a serum creatinine >2.5 mg/dL. Significant hepatic insufficiency defined as an SGPT (ALT) or SGOT (AST) >2.5 times the upper limit of normal. 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. Presence or history of drug or alcohol abuse. Prior exposure to ALT-711 or use of any other investigational drugs within 30 days prior to screening. Known seropositivity for HIV or hepatitis C, or presence of hepatitis B surface antigen. Severe COPD requiring recurrent oral steroids, oxygen at home or more than one inhaler. Baseline echocardiogram demonstrating the presence of left ventricular ejection fraction <50%. Unstable or uncontrolled myocardial ischemia, with no wall abnormality. 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. 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.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Dalane W Kitzman, MD
Organizational Affiliation
Associate Professor of Medicine and Cardiology, Wake Forest University Baptist Medical Center
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Michael R Zile, MD
Organizational Affiliation
Charles Ezra Daniel Professor of Medicine, Medical University of South Carolina
Official's Role
Principal Investigator
Facility Information:
Facility Name
Wake Forest University Baptist Medical Center, Department of Cardiology
City
Winston-Salem
State/Province
North Carolina
ZIP/Postal Code
27157-1045
Country
United States
Facility Name
Medical University of South Carolina and Ralph H. Johnson VA Medical Center
City
Charleston
State/Province
South Carolina
ZIP/Postal Code
29425 and 29401
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
10706607
Citation
Asif M, Egan J, Vasan S, Jyothirmayi GN, Masurekar MR, Lopez S, Williams C, Torres RL, Wagle D, Ulrich P, Cerami A, Brines M, Regan TJ. An advanced glycation endproduct cross-link breaker can reverse age-related increases in myocardial stiffness. Proc Natl Acad Sci U S A. 2000 Mar 14;97(6):2809-13. doi: 10.1073/pnas.040558497. Erratum In: Proc Natl Acad Sci U S A 2000 May 9;97(10):5679.
Results Reference
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PubMed Identifier
11527636
Citation
Hundley WG, Kitzman DW, Morgan TM, Hamilton CA, Darty SN, Stewart KP, Herrington DM, Link KM, Little WC. Cardiac cycle-dependent changes in aortic area and distensibility are reduced in older patients with isolated diastolic heart failure and correlate with exercise intolerance. J Am Coll Cardiol. 2001 Sep;38(3):796-802. doi: 10.1016/s0735-1097(01)01447-4.
Results Reference
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PubMed Identifier
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Citation
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Results Reference
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PubMed Identifier
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Citation
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Results Reference
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PubMed Identifier
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Citation
Kitzman DW. Heart Failure in the Elderly: Systolic and Diastolic Dysfunction. Am J Geriatr Cardiol. 1996 Jan;5(1):20-26. No abstract available.
Results Reference
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PubMed Identifier
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Citation
Little WC, Ohno M, Kitzman DW, Thomas JD, Cheng CP. Determination of left ventricular chamber stiffness from the time for deceleration of early left ventricular filling. Circulation. 1995 Oct 1;92(7):1933-9. doi: 10.1161/01.cir.92.7.1933.
Results Reference
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PubMed Identifier
9781977
Citation
Marburger CT, Brubaker PH, Pollock WE, Morgan TM, Kitzman DW. Reproducibility of cardiopulmonary exercise testing in elderly patients with congestive heart failure. Am J Cardiol. 1998 Oct 1;82(7):905-9. doi: 10.1016/s0002-9149(98)00502-5.
Results Reference
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PubMed Identifier
11158613
Citation
Vaitkevicius PV, Lane M, Spurgeon H, Ingram DK, Roth GS, Egan JJ, Vasan S, Wagle DR, Ulrich P, Brines M, Wuerth JP, Cerami A, Lakatta EG. A cross-link breaker has sustained effects on arterial and ventricular properties in older rhesus monkeys. Proc Natl Acad Sci U S A. 2001 Jan 30;98(3):1171-5. doi: 10.1073/pnas.98.3.1171.
Results Reference
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PubMed Identifier
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Citation
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Citation
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Citation
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Citation
Zile MR, Brutsaert DL. New concepts in diastolic dysfunction and diastolic heart failure: Part II: causal mechanisms and treatment. Circulation. 2002 Mar 26;105(12):1503-8. doi: 10.1161/hc1202.105290. No abstract available.
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Citation
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Citation
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Citation
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Citation
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The DIAMOND Study: Distensibility Improvement And Remodeling in Diastolic Heart Failure

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