Last updated on April 2018

A Safety and Efficacy Study of Dissolve in Treatment of Coronary In-stent Restenosis


Are you eligible to participate in this study?

You may be eligible for this study if you meet the following criteria:

  • Conditions: Coronary In-stent Restenosis
  • Age: Between 18 - 100 Years
  • Gender: Male or Female

Inclusion Criteria:

Related to the patients:

  1. Age 18 years old
  2. Patients who agree to accept the angiography follow-up visit at 9-month and follow up visits at 1-month, 6-month, 9-month, 1-year, 2-year, 3-year, 4-year and 5-year
  3. Patients with stable angina, unstable angina, old myocardial infarction or proven asymptomatic ischemia
  4. Patients who can receive any kind of coronary revascularization (including balloon angioplasty, stent implantation or coronary artery bypass grafting)

Related to lesion:

5. Restenosis after the first stent implant (including bare metal stents, stents with inert coating, and stents with active coating): Type Mehran I, Type II and Type III; the reference blood vessel diameter is 2.5 mm-4.0 mm, length 26mm

6. Before surgery, stenosis diameter must be 70% or 50% and accompanied by ischemia

7. The distance between other lesion requires interventional therapy and the target lesion must be > 10mm

8. One subject is allowed to have 2 target lesions at most, and 1 paclitaxel drug balloon for each lesion for dilation

9. Residual stenosis must be 30% after pre-dilatation, and dissection must be NHLBI type B

Exclusion Criteria:

Related to patients

  1. Pregnant or lactating women, or women who plan to get pregnant within 12 months or refuse to take effective contraceptives
  2. Patients with cardiogenic shock
  3. The patients had cerebral stroke within 6 months before being included, or have a history of peptic ulcer or gastrointestinal bleeding, or the patients have a bleeding tendency according to the investigator. Patients who are forbidden to use anticoagulation agents or anti-platelet drugs, and unable to tolerate aspirin or clopidogrel. Patients who are not able to tolerate and comply with dual antiplatelet therapy for at least 3 months after operation
  4. Patients who have Myocardial Infarction with thrombus or coronary slow flow symptoms and require immediate intervention
  5. Patients who had ST-Elevation Myocardial Infarction within 1 week before being included
  6. Patients with severe congestive heart failure or NYHA grade IV heart failure
  7. Patients with moderate or severe valvular heart disease
  8. Patients who had heart transplantation
  9. Patients with renal insufficiency (eGFR < 30mL/min)
  10. The patients have a life expectancy of less than 12 months, or it would be difficult to finish follow-ups within 12 months.
  11. The patients are participating in any other clinical trials before reaching the primary endpoints
  12. Patients who are unsuitable for the study according to the investigator due to other reasons

Related to the Lesion:

13. Patients with total occlusion at the target lesion

14. Lesion which cannot be treated by percutaneous transluminal coronary angioplasty (PTCA) or percutaneous intervention (PCI)

15. Reference vessel diameter < 2.0mm

16. Patients with multiple lesions ( 3) requiring percutaneous coronary intervention treatment in the same artery

17. 3-vessel disease that all need to be intervened

18. The diameter of the branch lesions in the target lesion 2.5mm

19. LM lesions and Ostial lesion within 5mm to the root aorta

20. Non-target lesion was not intervened successfully before target lesions being intervened

Related to concomitant therapy:

21. Patients cannot tolerate aspirin and/or clopidogrel and or tricagrelor, patients with the history of neutrocytopenia or thrombocytopenia, or patients with severe hypohepatia and prohibited to take clopidogrel

22. Patients known allergic to paclitaxel

23. Patients known allergic to contrast materials

Recruitment Status: Open


Brief Description Eligibility Contact Research Team


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