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NCT00760630 · ClinicalTrials.gov registry record
Measurements to Assess Severity of Epicardial Stenoses
A clinical trial, sponsored by University of Cincinnati.
- Terminated
- Registry status
- 10
- Enrollment target
NCT00760630 is a clinical trial that was terminated before completion, run by University of Cincinnati. The registered enrollment target is 10 participants.
The verdict
NCT00760630 was terminated before completion, sponsored by University of Cincinnati.
- TERMINATED
- Registry status
- 10 participants
- Enrollment target
Study Summary
Newly developed diagnostic parameters have potential to differentiate between epicardial disease and microvascular dysfunction with the help of anatomical details and physiological endpoints and can be used in present clinical settings.
Interventions
- DEVICE FFR/CFR and IVUS
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 10 participants |
| Start Date | 2009-12 |
| Est. Completion | 2012-02-24 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00760630
The ClinicalTrials.gov registry entry for NCT00760630 describes a study currently listed as terminated, categorized as an unspecified phase. The registered enrollment target is 10 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of Cincinnati, which has 245 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 1 intervention - of which FFR/CFR and IVUS is the first listed.
NCT00760630 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT00760630 about?
NCT00760630 is a clinical study titled "Measurements to Assess Severity of Epicardial Stenoses". Newly developed diagnostic parameters have potential to differentiate between epicardial disease and microvascular dysfunction with the help of anatomical details and physiological endpoints and can be used in present clinical settings.
What is the current status of trial NCT00760630?
This trial is currently terminated. The enrollment target is 10 participants. The study started on 2009-12. Estimated completion is 2012-02-24.
What interventions are being tested in trial NCT00760630?
The interventions under investigation include: FFR/CFR and IVUS (DEVICE).
Who is sponsoring clinical trial NCT00760630?
This trial is sponsored by University of Cincinnati, which has 245 total clinical trials registered on ClinicalTrials.gov.
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