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NCT01941030 · ClinicalTrials.gov registry record · NA
Complete Lesion Assessment With ffR and IVUS TechnologY
A NA study, sponsored by Abbott Medical Devices.
- Completed
- Registry status
- NA
- Development phase
- 51
- Enrollment target
NCT01941030 is a NA study that has completed, run by Abbott Medical Devices. The registered enrollment target is 51 participants.
The verdict
NCT01941030, a NA study, has completed, sponsored by Abbott Medical Devices.
- COMPLETED
- Registry status
- NA
- Development phase
- 51 participants
- Enrollment target
Study Summary
CLARITY I is a pilot study to identify the clinically appropriate endpoint(s) of a larger, statistically powered pivotal trial for treatment of patients with Critical Limb Ischemia (CLI).
Interventions
- DEVICE Balloon Angioplasty
- DEVICE Orbital Atherectomy System
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 51 participants |
| Start Date | 2013-03 |
| Est. Completion | 2015-06 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT01941030
The ClinicalTrials.gov registry entry for NCT01941030 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 51 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Abbott Medical Devices, which has 261 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 2 interventions - of which Balloon Angioplasty is the first listed.
NCT01941030 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT01941030 about?
NCT01941030 is a clinical study titled "Complete Lesion Assessment With ffR and IVUS TechnologY". CLARITY I is a pilot study to identify the clinically appropriate endpoint(s) of a larger, statistically powered pivotal trial for treatment of patients with Critical Limb Ischemia (CLI).
What is the current status of trial NCT01941030?
This trial is currently completed. It is a NA study. The enrollment target is 51 participants. The study started on 2013-03. Estimated completion is 2015-06.
What interventions are being tested in trial NCT01941030?
The interventions under investigation include: Balloon Angioplasty (DEVICE), Orbital Atherectomy System (DEVICE).
Who is sponsoring clinical trial NCT01941030?
This trial is sponsored by Abbott Medical Devices, which has 261 total clinical trials registered on ClinicalTrials.gov.
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