N/A
N=5
GRX With ReMOTE: First in Human in India
Percutaneous Coronary Intervention
Bottom Line
View on ClinicalTrials.gov: NCT03705481 ↗Enrolled (actual)
5
Serious AEs
0.0%
Results posted
Jan 2020
Primary outcome: Primary: Device Technical Success — 5 Participants
Study Design & Population
- Study type
- Interventional
- Phase
- N/A
- Interventions
- Remote treatment of PCI. (Device)
- Age
- Adult, Older Adult · 18+ yrs
- Sex
- All
- Sponsor
- Corindus Inc.
- Primary completion
- Dec 2018
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Device Technical Success |
5 | — |
| PRIMARY In-hospital MACE |
— | — |
| SECONDARY Clinical Procedural Success |
5 | — |
| SECONDARY All Serious Adverse Events |
— | — |
Summary
To evaluate the safety and performance of CorPath GRX POP System, in the ReMOTE (location outside hospital) delivery and manipulation of coronary guidewires and stent/balloon catheters, and manipulation of guide catheters during PCI procedures.
Eligibility Criteria
Inclusion Criteria
- Age ≥18 years;
- Patients with coronary artery disease with clinical indication for PCI;
- Patient deemed appropriate for robotic-assisted PCI; and
- The subject has been informed of the nature of the study, agrees to its provisions and has provided written informed consent.
Angiographic Inclusion:
- Study lesion is a single de novo native coronary artery lesion (i.e. a coronary lesion not previously treated).
- The lesion reference vessel diameter is between 2.50 mm and 4.0 mm by visual estimate.
- Study lesion length less or equal to 20 mm by visual estimate.
- The study lesion length can be treated with one stent. The stent should be able to cover the whole length of the lesion with at least 2 mm of normal segments on proximal and distal edges of the lesion.
- Study lesion diameter showing significant stenosis of at least 50% by visual estimate.
Exclusion Criteria
- Failure/inability/unwillingness to provide informed consent; or
- The investigator determines that the patient or the coronary anatomy is not suitable for robotic-assisted PCI.
Angiographic Exclusion:
- Target lesion that cannot be fully covered by a single stent.
- Subject requires treatment of multiple lesions
- Any previous stent placement within 5 mm (proximal or distal) of the target lesion
- The study lesion requires planned treatment with DCA, laser, rotational atherectomy, or any device except for balloon dilatation prior to stent placement
- The study vessel has evidence of intraluminal thrombus or moderate to severe tortuosity (> 90°) proximal to the target lesion
- The study lesion has any of the following characteristics:
- Total occlusion
- Within 2mm of a side branch > 2.0 mm vessel diameter
- Not ostial in location
- Is located at ≥ 45° bend in the vessel
- Is severely tortuous
- Is severely calcified
- Severe calcification at the part of the vessel proximal to target lesion
- Target lesion that is located in a native vessel distal to an anastomosis with a saphenous vein graft or a left/right internal mammary artery (LIMA/RIMA) bypass and is approached through the by-pass graft
- Unprotected left main coronary artery disease (an obstruction greater than 50% diameter stenosis in the left main coronary artery)
Data sourced from ClinicalTrials.gov (NCT03705481). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.