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Completed

NCT Number: NCT02140801

Optical Coherence Tomography to Evaluate Ticagrelor and Clopidogrel

A number of 352 patients scheduled for elective percutaneous coronary intervention (PCI) with a native coronary stenosis suitable for DES implantation and OCT imaging are openly randomized 1:1 to either BRILINTA™ (ticagrelor) or Plavix® (clopidogrel bisulfate).

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 4

Primary location

Nanjing First Hospital

Nanjing, Jiangsu, 210006, China

About this study

The study is prospectively conducted at 4 high-volume PCI center in China with OCT expertise. Angiographic follow-up and OCT imaging with motorized pull-back at 20-36 mm/s are planned in all patients 12 months after implantation of the study stents. OCT endpoints are: (1) Subclinical intra-stent thrombus, defined as a mass protruding to the lumen with significant attenuation, and respectively (2) endothelial coverage, expressed as % of struts without coverage and % of stent length containing non-covered struts. The study is powered for OCT endpoints, which are likely to reach significance at the level P < 0.05 even at a follow-up drop-out rate up to 10%.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Provision of informed consent prior to any study specific procedures;
  • Men and women 18 years and older;.
  • Established indication to PCI according to the guidelines of American Heart Association and American College of Cardiology;
  • Native coronary lesion suitable for drug-eluting stent placement and OCT imaging.

Exclusion criteria

  • Pregnancy and breast feeding mother;
  • Co-morbidity with an estimated life expectancy of < 50 % at 12 months;
  • Scheduled major surgery in the next 6 months;
  • Inability to follow the protocol and comply with follow-up requirements or any other reason that the investigator feels would place the patient at increased risk;
  • Previous enrolment in this study or treatment with an investigational drug or device under another study protocol in the past 30 days
  • Cardiogenic shock
  • Previous subacute or late coronary stent thrombosis
  • Known allergy against ticagrelor, or against clopidogrel, or aspirin
  • History of major hemorrhage (intracranial, gastrointestinal, etc.)
  • Active pathological bleeding
  • Acute or chronic hematologic disorder including a Hemoglobin less than 10 g/L or a platelet count less than 10×109/L before procedure
  • Any history of Severe renal or hepatic dysfunction (hepatic failure, cirrhosis, portal hypertension and active hepatitis);
  • Neutropenia,
  • thrombocytopenia;
  • Known acute pancreatitis
  • Arterial aneurysm, arterial/venous malformation and aorta dissection.
  • Culprit lesion within the proximal 10 mm of the right or left coronary artery
  • Saphenous vein grafts
  • Lesion length > 30 mm
  • Involves a side branch ≥2.0 mm in diameter by visual estimate which requires treatment
  • In-stent restenotic lesions
  • Thombus-containing lesions

Treatment and study plan

Ticagrelor

Drug

Plain, round, yellow, filmcoated tablet, 90 mg

Other names: BRILINTA™

clopidogrel

Drug

Orange brown capsule, containing one 75 mg clopidogrel tablet (cut into 2 halves)

Other names: Plavix®

Primary outcomes

  1. Subclinical thrombus

    Time frame: 12 months

    The occurrence of subclinical thrombus as detected by OCT

Secondary outcomes

  1. Endothelial coverage of the stent struts assessed by optical coherence tomography

    Time frame: 12 months

  2. Neointimal proliferation within the stent assessed by optical coherence tomography

    Time frame: 12 months

  3. Stent malposition assessed by optical coherence tomography

    Time frame: 12 months

  4. Edge dissections assessed by optical coherence tomography

    Time frame: 12 months

Other outcomes

  1. Bleeding events

    Time frame: 12 months

Sponsors and collaborators

Lead sponsor

Nanjing First Hospital, Nanjing Medical University

Other

Registry information

Official study title

A Randomised, Open-label, Parallel Group, Multi-center Study Using OCT to Comparing the Efficacy and Safety of Ticagrelor With Clopidogrel in the Prevention of Subclinical Thrombus in Patients After Drug-eluting Stent Implantation

Important dates

Study start
2014
Primary completion
2017
Study completion
2017
First posted
May 16, 2014
Registry last updated
Mar 21, 2018

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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