Study to Evaluate the Safety and Effectiveness of MynxGrip Vascular Closure Device

A Multicenter, Open Label, Prospective, Randomized Study of the MynxGrip Vascular Closure Device in Subjects With Diagnostic or Interventional Endovascular Procedures (PANDA Study)

To evaluate the safety and effectiveness of MynxGrip, in hemostasis of common femoral artery puncture site, compared with manual compression hemostasis in patients who have undergone diagnostic or interventional endovascular procedures utilizing a 5F, 6F or 7F procedural sheath.

Effectiveness: to superiority to the control group in time to hemostasis. Comparison of time to ambulation, procedure success rate, length of stay in hospital, device success rate.

Safety-Major/Minor complication rate, adverse events, SAEs as compared to control.

Inclusion Criteria:

1. Patients ≥ 18 years of age;
2. Patients who are able and willing to sign the informed consent form;
3. Patients who agree to follow all study visits and procedures;
4. Patients who plan to receive the diagnostic or interventional endovascular procedures via percutaneous common femoral artery puncture;
5. Patients who are able to walk, as judged by the investigators.

Exclusion Criteria:

1. Patients are proved to have clinically significant peripheral vascular disease according to any of the following situations:

   1. Patients showing severe claudication after walking less than 200 meters,
   2. No palpable pulse on the patients' affected limbs,
   3. Patients having received surgical procedures involving the ipsilateral common femoral artery
   4. Patients having received percutaneous transluminal angioplasty (PTA), stent placement, or vascular graft in the ipsilateral common femoral artery;

2. Patients with morbid obesity (BMI > 40 kg/m2);

3. Patients with a myocardial infarction (MI) with acute elevated ST segment ≤24 hours prior to procedure;

4. Patients with the prior procedure in the ipsilateral common femoral artery ≤30 days;

5. Patients having received ipsilateral vascular closure device;

6. Patients with bleeding disorders such as thrombocytopenia (platelet count < 100,000/ mm3), hemophilia, von Willebrand disease or severe anemia (Hgb < 10 g/dL, Hct < 30%);

7. Patients with documented INR > 1.5 or patients currently receiving glycoprotein IIb/IIIa platelet inhibitors;

8. Patients with symptoms of local infection or inflammation in the groin;

9. Patients who are participating in any other clinical studies on drugs or medical devices at the same time;

10. Patients who are pregnant or in lactation;

11. Patients with known allergy to contrast medium;

12. Patients with known allergy to polyethylene glycol;

13. Patients with treated but still uncontrolled hypertension (systolic pressure>180 mmHg or diastolic pressure>110 mmHg);

14. Patients with known autoimmune diseases;

15. Patients who are receiving long-term corticosteroid therapy;

16. Patients with expected life of less than 30 days;

17. Patients with unilateral or bilateral lower-extremity amputation;

18. Patients who can't walk 6 meters (20 steps) without a support for any reason;

19. Patients requiring prolonged length of stay [For example, the patient will receive the coronary artery bypass grafting (CABG) or the patient plans to receive the CABG ≤30 days after the surgery];

20. Patients with mental disorders and cognitive impairment;

21. Patients have participated into this study before; Intra-operative exclusion criteria;

22. Patients with treated but still uncontrolled hypertension (systolic pressure>180 mmHg or diastolic pressure>110 mmHg);

23. Patients implanted with a balloon pump inside the aorta;

24. Patients whose common femoral artery is too thin (<5 mm in diameter);

25. Patients with obviously fibrotic, calcified, or >50% stenotic femoral artery;

26. Patients having received puncture at other artery than the common femoral artery;

27. Patients having received antegrade puncture;

28. Patients having received arterial puncture at a number of different sites or who are suspected to have received posterior femoral arterial wall puncture;

29. Patients implanted with ipsilateral venous sheath;

30. Surgical findings or complications which the investigators consider may interfere with the patients' participation into the study (For example, the sheath deployment is difficult due to the scar, tortuous vessels, or use of the sheath with the other sizes than 5 Fr, 6 Fr or 7 Fr, or the sheath with the total length of >15.7 cm);

31. Patients with preexisting hematoma, intraluminal thrombus, pseudoaneurysm, AV Fistula or any type of dissection;

32. Patients requiring prolonged length of stay [For example, the patient will receive the coronary artery bypass grafting (CABG) or the patient plans to receive the CABG ≤30 days after the surgery];

33. Patients who are included in another drug or medical device study.