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CARDIOLITE-413: A Study for Patients Who Had a PCI for an Acute MI

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Lantheus Medical Imaging

Status and phase

Completed
Phase 4

Conditions

Myocardial Infarction

Treatments

Drug: Technetium Tc99m Sestamibi

Study type

Interventional

Funder types

Industry

Identifiers

NCT00162331
CARDIOLITE-413

Details and patient eligibility

About

The purpose of this clinical study is to learn if there are any changes in how blood gets to your heart muscle and if your heart size changed after your heart attack.

Enrollment

74 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Undergoing primary or rescue PCI for acute MI with ECG evidence of a large territory at risk.

Exclusion criteria

  • History of prior MI or CABG surgery, persistent LBBB, Atrial Fibrillation, End stage renal disease, Weight > 350 lbs.

Trial design

Primary purpose

Diagnostic

Allocation

Non-Randomized

Interventional model

Single Group Assignment

Masking

None (Open label)

Trial contacts and locations

8

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Data sourced from clinicaltrials.gov

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