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RISE: A Clinical Evaluation of the StarClose™ Vascular Closure System
NCT00736086 · View on ClinicalTrials.gov ↗
Study Summary
To evaluate early ambulation in patients who receive the StarClose™ VCS post-percutaneous diagnostic procedure.
Conditions Studied
Interventions
- DEVICE Vessel Closure (StarClose™)
Study Locations (11)
New York
- New York Methodist Hospital — Brooklyn
- Buffalo Heart group — Buffalo
California
- Scripps Memorial Hospital — La Jolla
Georgia
- Fuqua Heart Center/ Piedmont Hospital — Atlanta
Illinois
- Heart Care Midwest (OSF/St Francis) — Peoria
Indiana
- The Care Group LLC (St. Vincent's Hospital) — Indianapolis
Michigan
- Bay Regional Medical Center — Bay City
Minnesota
- Minneapolis Heart Institute Foundation/Abbott Northwestern Hospital — Minneapolis
Missouri
- St. Luke's Hospital — Kansas City
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 165 participants |
| Start Date | 2006-03 |
| Est. Completion | 2006-12 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00736086
The ClinicalTrials.gov registry entry for NCT00736086 describes a study currently listed as completed. It is categorized as an unspecified phase, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 165 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Abbott Medical Devices, which has 155 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 2 conditions, with Cardiovascular Disease appearing as the primary indexed condition, and to 1 intervention — of which Vessel Closure (StarClose™) is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.
Geographic footprint matters for practical reasons: NCT00736086 reports 11 study locations spanning 10 distinct geographic areas — top geographies include New York, California, Georgia. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.
Frequently Asked Questions
What is clinical trial NCT00736086 about?
NCT00736086 is a clinical study titled "RISE: A Clinical Evaluation of the StarClose™ Vascular Closure System". To evaluate early ambulation in patients who receive the StarClose™ VCS post-percutaneous diagnostic procedure.
What is the current status of trial NCT00736086?
This trial is currently completed. The enrollment target is 165 participants. The study started on 2006-03. Estimated completion is 2006-12.
What conditions does trial NCT00736086 study?
This clinical trial studies the following conditions: Cardiovascular Disease, Peripheral Vascular Disease. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT00736086?
The interventions under investigation include: Vessel Closure (StarClose™) (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT00736086?
This trial is sponsored by Abbott Medical Devices, which has 155 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT00736086 being conducted?
This trial has 11 study locations across California, Georgia, Illinois, Indiana, Michigan. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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