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Phase II Clinical Trial to Evaluate the Benefits of Postconditioning in ST-Elevation Myocardial Infarction (STEMI)

This study is ongoing, but not recruiting participants.
Sponsor:
Collaborator:
National Heart, Lung, and Blood Institute (NHLBI)
Information provided by (Responsible Party):
Minneapolis Heart Institute Foundation
ClinicalTrials.gov Identifier:
NCT01324453
First received: March 25, 2011
Last updated: January 24, 2017
Last verified: January 2017
March 25, 2011
January 24, 2017
March 2011
November 2016   (Final data collection date for primary outcome measure)
  • Infarct size on baseline cMRl [ Time Frame: Day 3-5 post-PCI ]
  • Myocardial Salvage Index (MSI) on baseline cMRI [ Time Frame: Day 3-5 post-PCI ]
  • Micro vascular Obstruction (MVO) on baseline cMRI [ Time Frame: Day 3-5 post-PCI ]
  • Infarct size on baseline cMRl [ Time Frame: Day 3-5 post-PCI ]
  • Myocardial Salvage Index (MSI) on baseline cMRI [ Time Frame: Day 3-5 post-PCI ]
  • Micro vascular Obstruction (MVO) on baseline cMRI [ Time Frame: Day 3-5 post-PCI ]
  • Plasma levels of reactive oxidative stress chemicals: 8-isoprostane and MDA (ROS) [ Time Frame: pre and post-reperfusion ]
Complete list of historical versions of study NCT01324453 on ClinicalTrials.gov Archive Site
  • Global Left Ventricular Ejection Fraction [ Time Frame: baseline ]
  • Infarct size by CK and troponin peak [ Time Frame: over the first 24 hours post pci ]
  • LV Remodeling (LVEDV) as measured by cMRl [ Time Frame: baseline ]
  • LV Remodeling (LVESV) as measured by cMRl [ Time Frame: baseline ]
  • Global Left Ventricular Ejection Fraction [ Time Frame: baseline, 3 and 12 months ]
  • Infarct size by CK and troponin area under the curve [ Time Frame: over the first 72 hours post pci ]
  • LV Remodeling (LVEDV, LVESV) as measured by cMRl [ Time Frame: baseline and 3 and 12 months ]
  • Plasma and whole blood levels of chemical compounds altered by complete artery occlusion: nitrite anion and hydrogen sulfide [ Time Frame: pre and post-reperfusion ]
Not Provided
Not Provided
 
Phase II Clinical Trial to Evaluate the Benefits of Postconditioning in ST-Elevation Myocardial Infarction (STEMI)
Phase II Clinical Trial to Evaluate the Benefits of Postconditioning in STEMI
This study will evaluate change in heart muscle function from baseline to three months and twelve months in participants who present with a heart attack and a completely occluded coronary artery. These subjects will be randomized to receive standard Percutaneous transluminal coronary angioplasty (PTCA)/Stenting to open the artery or routine PTCA/Stenting plus post conditioning. Post conditioning commences immediately upon reperfusion using four cycles of thirty second inflations with a standard angioplasty balloon followed by a thirty seconds of reperfusion. The investigators hypothesize that Postconditioning reduces the size of the heart attack when utilized with successful primary Angioplasty/stent.
Single center study involving 140 patients randomized to Post Conditioning + Percutaneous coronary intervention (PCI) versus routine PCI during their ST-Elevation Myocardial Infarction (STEMI, Heart Attack) presentation. The Post Conditioning protocol consists of performing four, 30-second PTCA (Angioplasty) balloon occlusions followed by 30-seconds of reperfusion over a total of 4 minutes. The first balloon inflation occurs immediately after an angioplasty guidewire is placed through the obstruction in the artery. Following this protocol the vessel is stented as part of the usual practice for treatment of STEMI. No other treatment differences will occur between the two groups and all patients will receive the usual post-STEMI care. Patients in both groups will receive a cardiac MRI 3-5 days following their STEMI for measurement of heart attack size and heart muscle function, among other measures. Patients will undergo collection of blood for CK MB and troponin I every 8 hours for 24 hours following PCI. All patients will be followed by phone follow-up visits to review history and MACE (death, recurrent STEMI, repeat revascularization, arrhythmias, ICD placement and hospitalization for CHF). All patients will be required to take P2Y12 inhibitors and aspirin for the duration of the trial. All patients will be treated with ACEI, beta blockers and statins.
Interventional
Phase 1
Phase 2
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: No masking
Primary Purpose: Treatment
Acute Myocardial Infarction
  • Procedure: Post Conditioning + Primary PCI
    Four, 30-second PTCA balloon occlusions followed by 30-seconds of reperfusion over a total of 4 minutes, in addition to Percutaneous Coronary Intervention as clinically indicated.
  • Procedure: Standard Primary PCI
    Routine Percutaneous Coronary Intervention as clinically indicated.
  • Experimental: Post conditioning + PCI
    Intervention: Procedure: Post Conditioning + Primary PCI
  • Active Comparator: Standard PCI
    Intervention: Procedure: Standard Primary PCI
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Active, not recruiting
140
March 2019
November 2016   (Final data collection date for primary outcome measure)

Inclusion Criteria:

  • Age > 18 years old, < 80 years old
  • Able to give informed consent
  • Able to undergo cMRl
  • ST-segment elevation infarction with 100% occlusion of a major epicardial vessel (> 2.5 mm)
  • No angiographic evidence of collateral flow distal to occluded artery
  • Ischemic duration between 1.0 and 6 hours
  • TIMI 3 Flow following PCI

Exclusion Criteria:

  • Visible collateral blood flow to the distal vasculature of the occluded vessel
  • Previous Coronary Artery Bypass Graft surgery
  • Previous q-wave myocardial infarction in the same territory
  • Inability to give informed consent
  • Inability to undergo cMRl
  • Life expectancy less than one year
  • History of Non-compliance or alcohol or drug addiction
  • Patients with cardiogenic shock, cardiac arrest, hypothermia on presentation
  • Chronic dialysis or significant renal insufficiency (CrCl < 35 mI/mm/i .73 m2)
  • TIMI Flow > 0 on presentation
  • Ischemic Time > 6 hours or < 1.0 hours
  • Presence of significant valvular heart disease (>mod AS, >2+ MR)
  • Known LV systolic dysfunction (LVEF < 50% prior to STEMI)
Sexes Eligible for Study: All
18 Years to 80 Years   (Adult, Senior)
No
Contact information is only displayed when the study is recruiting subjects
United States
 
 
NCT01324453
opt004
1R01HL103927-01A1 ( U.S. NIH Grant/Contract )
Yes
Not Provided
Not Provided
Minneapolis Heart Institute Foundation
Minneapolis Heart Institute Foundation
National Heart, Lung, and Blood Institute (NHLBI)
Principal Investigator: Jay H Traverse, MD Minneapolis Heart Institute Foundation at Abbott Northwestern Hospital
Minneapolis Heart Institute Foundation
January 2017

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