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NCT00381316 · ClinicalTrials.gov registry record · Phase 4

Comparison of Diagnostic Rest/Stress SPECT Results for Patients With Myocardial Ischemia and Infarction Using Myoview in Both Single and Dual Isotope Acquisition Approaches

A Phase 4 study, sponsored by GE Healthcare.

Completed
Registry status
Phase 4
Development phase
291
Enrollment target

NCT00381316: Completed Phase 4 study, sponsored by GE Healthcare.

NCT00381316 is a Phase 4 study that has completed, run by GE Healthcare. The registered enrollment target is 291 participants, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (44% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00381316, a Phase 4 study, has completed, sponsored by GE Healthcare.

COMPLETED
Registry status
Phase 4
Development phase
291 participants
Enrollment target

Study Summary

The study is designed to determine whether a dual isotope protocol is equivalent to a single isotope in the diagnosis of myocardial ischemia and infarction using MYOVIEW SPECT imaging.

Interventions

  • DRUG Technetium Tc99m Tetrofosmin injections
  • DRUG Thallous Chloride T1-201

Trial Details

FieldValue
Enrollment Target 291 participants
Start Date 2006-07
Est. Completion 2006-12
Phase Phase 4
GE Healthcare

99 total trials

What the finished NCT00381316 record still lists

NCT00381316 is an interventional study that assigns participants to a tested intervention. The registered 291 participants enrollment target is mid-sized for trials with a published cap, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (44% lower).

The record links to 0 conditions, and to 2 interventions - of which Technetium Tc99m Tetrofosmin injections is the first listed.

NCT00381316 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00381316 about?

NCT00381316 is a clinical study titled "Comparison of Diagnostic Rest/Stress SPECT Results for Patients With Myocardial Ischemia and Infarction Using Myoview in Both Single and Dual Isotope Acquisition Approaches". The study is designed to determine whether a dual isotope protocol is equivalent to a single isotope in the diagnosis of myocardial ischemia and infarction using MYOVIEW SPECT imaging.

What is the current status of trial NCT00381316?

This trial is currently completed. It is a Phase 4 study. The enrollment target is 291 participants. The study started on 2006-07. Estimated completion is 2006-12.

What interventions are being tested in trial NCT00381316?

The interventions under investigation include: Technetium Tc99m Tetrofosmin injections (DRUG), Thallous Chloride T1-201 (DRUG).

Who is sponsoring clinical trial NCT00381316?

This trial is sponsored by GE Healthcare, which has 99 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00381316's enrollment target sits among peer trials

291 297th of 2000 higher than 1,704 of 2,000 other Phase 4 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 4 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT00381316, the US trial registry maintained by the National Library of Medicine. NCT00381316 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.