CorPath GRX STEMI Study
NCT04459299 · Status: TERMINATED · Type: OBSERVATIONAL · Enrollment: 3
Last updated 2023-12-20
Summary
This study will evaluate the performance of the CorPath GRX System in Robotic Primary PCI (RPPCI) in the treatment of ST-elevated myocardial infarction (STEMI).
Conditions
- STEMI - ST Elevation Myocardial Infarction
- CAD
Interventions
- DEVICE
-
Robotic-PCI (CorPath GRX System)
Robotic-PCI for acute ST elevation myocardial infarction (STEMI).
Sponsors & Collaborators
-
Corindus Inc.
lead INDUSTRY
Principal Investigators
-
Salvatore F Mannino, DO, MA · WellStar Health System
Eligibility
- Min Age
- 18 Years
- Max Age
- 80 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2020-09-28
- Primary Completion
- 2020-11-26
- Completion
- 2020-11-29
- FDA Device
- Yes
Countries
- United States
Study Locations
More Related Trials
-
PRECISION GRX Registry
NCT03278301 ·Status: COMPLETED
-
Cardiac Cath Lab Staff Radiation Exposure
NCT03959072 ·Status: TERMINATED
-
The ROB-OSTIAL Study
NCT05634538 ·Status: TERMINATED ·Phase: NA
-
Post-Market CorPath Registry on the CorPath 200 System in Percutaneous Coronary Interventions
NCT01917682 ·Status: COMPLETED
-
GRX With ReMOTE: First in Human in India
NCT03705481 ·Status: COMPLETED ·Phase: NA
-
MicroNet-covered Stent System for Stroke Prevention in All Comer Carotid Revascularization
NCT04271033 ·Status: RECRUITING ·Phase: NA
-
CorMatrix ECM for Carotid Repair Following Endarterectomy Registry
NCT01569594 ·Status: COMPLETED
-
Robotic-Assisted Peripheral Intervention for Peripheral Arterial Disease II
NCT02742077 ·Status: COMPLETED ·Phase: NA
-
Evaluation of the GTX™ 5126 DES Coronary Stent System in the Treatment of Patients With a Lesion in the Coronary Artery
NCT00777842 ·Status: TERMINATED ·Phase: NA
-
VasoStar Vibrational Guidewire System to Facilitate Crossing Coronary Artery Chronic Total Occlusions
NCT06193954 ·Status: RECRUITING ·Phase: NA
-
Safety and Efficacy of the CGuard™ Carotid Stent System in Carotid Artery Stenting
NCT04900844 ·Status: ACTIVE_NOT_RECRUITING ·Phase: NA
-
The Asahi Intecc PTCA Chronic Total Occlusion Study
NCT02379923 ·Status: COMPLETED ·Phase: NA
-
TCAR Cerebral Protection And MicroNET-Covered Stent To Reduce Strokes
NCT04547387 ·Status: UNKNOWN
-
Feasibility Study of the DragonFire for Hypertrophic Obstructive Cardiomyopathy
NCT06368037 ·Status: NOT_YET_RECRUITING ·Phase: NA
-
Evaluation of the TriActiv ProGuard System During Carotid Artery Stenting
NCT00395785 ·Status: TERMINATED ·Phase: PHASE2/PHASE3
-
DXR Stent(Previous Cilotax) Implantation Registry
NCT01612819 ·Status: TERMINATED
-
Clinical Study to Evaluate the Safety and Effectiveness of MER® Stents in Carotid Revascularisation.
NCT03133429 ·Status: COMPLETED ·Phase: NA
-
Study on the Trans-Carotid Artery Occlusion Shunt System Combined With Introducer Sets
NCT06959628 ·Status: RECRUITING ·Phase: NA
-
Prospective Study of the SoundBite™ Crossing System in Complex Peripheral CTOs
NCT03933657 ·Status: WITHDRAWN ·Phase: NA
-
Early Feasibility Study of the Supira System in Patients Undergoing HRPCI
NCT06087575 ·Status: COMPLETED ·Phase: NA
-
GORE Embolic Protection With Reverse Flow
NCT00594100 ·Status: COMPLETED ·Phase: PHASE3
-
Shockwave Coronary Lithoplasty Study
NCT02758379 ·Status: COMPLETED ·Phase: NA
-
RevCore for In Stent Thrombosis
NCT06394739 ·Status: RECRUITING
-
RESOLUTE ONYX Post-Approval Study
NCT03063749 ·Status: COMPLETED
-
Acolyte CTO-PCI Study: Imaging and Catheter System to Treat Patients With Coronary Chronic Total Occlusion, Who Have Persistent Symptoms Following Medical Therapy and Are Undergoing Percutaneous Coronary Interventional Procedures
NCT06795763 ·Status: ENROLLING_BY_INVITATION ·Phase: NA