A Clinical Study for the Pan-vascular Interventional Robotic System

Percutaneous Coronary Intervention Clinical Trial

Official title:

A Clinical Study for Pan-vascular Interventional Control System in Percutaneous Coronary Intervention

Clinical Trial Details — Status: Not yet recruiting

Administrative data

• NCT number: NCT06110988
• Other study ID #: P02-IIT-KSI
• Status: Not yet recruiting
• Phase: N/A
• Start date: April 30, 2024
• Est. completion date: September 30, 2024

Study information

• Verified date: April 2024
• Source: Shenzhen Institute of Advanced Biomedical Robot Co., Ltd.
• Contact: Qingxing Chen, MD
• Phone: 18999090210
• Email: sunjiabao[@]abrobo.com
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The goal of this prospective, single-center, single-arm study is to explore the efficacy and safety of the pan-vascular interventional robotic system for percutaneous coronary intervention (PCI), researchers will assess the clinical success, technical success, and record the intraoperative data (PCI time, guidewire operation time, dose of contrast medium, radiation exposure doses, etc). All subjects will be followed up on the day of surgery, before discharge (or 48 hours after surgery) and 1 month after surgery to observe the safety indicators.

Recruitment information / eligibility

• Status: Not yet recruiting
• Enrollment: 5
• Est. completion date: September 30, 2024
• Est. primary completion date: September 30, 2024
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 80 Years

Eligibility

Inclusion Criteria:

1. General Inclusion criteria:

1. 18 years old = age =80 years old;

2. have a clinical indication for PCI (clinical evidence of ischemic heart disease or a positive functional study);

3. Subjects or their legal representative has been informed of the nature of the study, signed informed consent and were willing to cooperate in the follow-up.

2. Angiographic inclusion criteria:

1. study lesion is a single de novo native coronary artery lesion (previously untreated coronary artery disease);

2. target vessel diameter between 2.5 mm and 4.0 mm;

3. single lesion length =38 mm, with at least 2.0 mm normal segments on the proximal and distal edges of the lesion;

4. stenosis =50% and < 100%.

Exclusion Criteria:

1. General exclusion criteria:

1. hemodynamic instability (including hypotension or use of vasopressors to maintain blood pressure);

2. STEMI, cardiopulmonary resuscitation, or cardiogenic shock within 7 days before surgery;

3. subjects were required to undergo planned PCI or CABG within 30 days after surgery, or had undergone PCI within 72 hours before surgery, or had undergone PCI within 30 days before surgery with a protocol-defined major adverse coronary event (MACE) or serious adverse event (SAE);

4. subjects had a stroke or transient ischemic attack (TIA) within 30 days before surgery;

5. subjects with active peptic ulcer or upper GI bleeding within 6 months before surgery;

6. The study lesion requires planned treatment with directional coronary atherectomy (DCA), laser, rotational atherectomy or any device except for balloon dilatation prior to stent placement

7. left ventricular ejection fraction (LVEF) < 35%;

8. subjects with known allergies to or contraindications to antiplatelet drugs, anticoagulants, stent materials and their coatings, or allergies to contrast agents, unable to receive adequate preoperative medication or manage with clinically appropriate alternatives;

9. subjects had a history of bleeding tendency or coagulopathy or refused blood transfusion;

10. severe liver and kidney dysfunction;

11. patients who are scheduled to undergo additional cardiac surgery (e.g., valve replacement or cardiac ablation) within 30 days after surgery;

12. inaccessible vascular access (radial artery/femoral artery) or severe vascular stenosis, occlusion or skin infection at the puncture site;

13. uncontrolled severe infection;

14. subjects participating in clinical studies of other devices or drugs during the same period;

15. pregnant and lactating women of childbearing age;

16. subjects judged by the investigator to be ineligible for the study.

2. Exclusion criteria for angiography:

1. in-stent restenosis or any previous stent placement within 5.0 mm (proximal or distal) of the target lesion;

2. bifurcation lesions, in which the target vessel branch needs to be protected but cannot be protected;

3. the target lesion is located at the ostium or anastomosis of coronary artery;

4. investigate evidence of intravascular thrombosis;

5. severe tortuosity or calcification of the proximal end of the study vessel or target lesion;

6. study the complete occlusion of the lesion;

7. Target lesion located in left main coronary artery, or unprotected left main coronary artery disease (> 50% stenosis in left main coronary artery).

Related Conditions & MeSH terms

• Percutaneous Coronary Intervention

Intervention

Device:
• Pan-vascular interventional robotic system
Pan-vascular interventional robotic system assited PCI for delivery and manipulation of guidewires, catheters, and quick exchange balloon dilatation catheters/stents.

Locations

Country	Name	City	State
China	Kashi Prefecture Second People's Hospital	Kashgar	Xinjiang
China	Shanghai Zhongshan Hospital	Shanghai	Shanghai

Sponsors (1)

Lead Sponsor	Collaborator
Shenzhen Institute of Advanced Biomedical Robot Co., Ltd.

Country where clinical trial is conducted

China, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Clinical Success	Less than 30% residual stenosis (visual estimate) post PCI in the lesion(s) treated with the Pan-vascular interventional robotic system, without in-hospital major adverse coronary events (MACE).	Discharge or 48 hours post intervention, whichever comes first
Primary	Technical Success	Defined as successful completion of the robotic-assisted PCI absent unplanned conversion to manual for guidewire or balloon/stent catheter inability to navigate vessel anatomy or poor guide catheter support.	Procedure
Secondary	Procedure Time	Defined as the time measured from the insertion of the hemostasis sheath until the removal of the guide catheter.	Procedure
Secondary	PCI time	Defined as the time measured from the insertion of the guide catheter until the removal of the guide catheter.	Procedure
Secondary	Fluoroscopy Time	Total Fluoroscopy Time during procedure will be captured	Procedure
Secondary	Radiation Exposure	Patient and Main operator radiation exposure dose recorded by portable radiation monitor during the procedure, respectively.	Procedure
Secondary	Contrast agent dosage	The total amount of contrast agent used during the whole procedure.	Procedure