Routinely Deferred Versus Early Intervention in Elderly Patients With Non-ST-elevation Myocardial Infarction

Non-ST Elevation Myocardial Infarction Clinical Trial

— DEAR-OLD  

Official title:

Routinely Deferred Versus Early Invasive Strategy in Chinese Patients of 75 Years or Older With Non-ST-elevation Myocardial Infarction - a Multicenter, Open-label, Randomized Controlled Clinical Trial.

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT02900001
• Other study ID #: LHJJ201510626
• Status: Recruiting
• Phase: N/A
• First received: August 24, 2016
• Last updated: September 29, 2017
• Start date: December 1, 2016
• Est. completion date: October 30, 2019

Study information

• Verified date: September 2017
• Source: Chinese Academy of Medical Sciences, Fuwai Hospital
• Contact: Jingang Yang, M.D.
• Phone: +86-13810821420
• Email: yangjingang[@]126.com
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This study is to evaluate the efficacy and safety of a routinely deferred invasive strategy in comparison with an early invasive strategy in Chinese elderly patients of 75 years or older with non-ST elevation myocardial infarction, aiming to test the hypothesis that routinely deferred invasive strategy is not inferior to early invasive strategy in such an elderly group of patients.

Description:

This study aims to enroll 696 elderly patients with non-ST elevation myocardial infarction (NSTEMI) from 20 hospitals throughout mainland China.. Consective patients of 75 years or older with a diagnosis of NSTEMI will be suitable for enrollment. Written informed consent form will be obtained from every patients. Initially stabilized patients with an ischemic episode within 24 hours before admission will be randomized and others will be registered. For randomization, the patients' brief information will be entered in a central randomization system to generate a random number.

According to the random number, each patient will be randomly assigned to early invasive therapy versus routinely deferred invasive strategy. All patients will initiate dual antiplatelet therapy (aspirin+P2Y12 inhibitor) and continued till the end of follow-up at one year. For patients assigned to early invasive group, a loading dose of antiplatelet agent should be given, unless contraindicated. Anticoagulation, anti-ischemic agents, statin and other guideline recommended medicine will be given according to physician in charge according to guideline.

Patients assigned to early invasive strategy will undergo coronary angiography within 24 hours after admission and have percutaneous coronary intervention or coronary artery bypass grafting as soon as possible during the index hospitalization if appropriate. Patients assigned to deferred invasive strategy will undergo coronary angiography and subsequent revascularization after at lest 72 hours after admission and in the index hospitalization. Patients who undergo percutaneous coronary intervention can receive a glycoprotein IIb/IIIa inhibitor if indicated and upfront use of glycoprotein IIb/IIIa inhibitors is discouraged. The choice of intervention or surgery and the choice of complete or staged revascularization will be determined by the operator according to coronary anatomy and consistent with current practice guidelines. Patients assigned to deferred strategy should undergo urgent coronary angiography and revascularization accordingly if indicated during the period of time waiting for catheterization. Such procedure will be adjudicated as an endpoint. Elective percutaneous coronary intervention on non-culprit vessels, in either study arm, can take place sometime after the index procedure with the goal to achieve complete revascularization. Such staged procedures will not be deemed as an adverse event.

Specific data for acquisition:

Research demographics: age, height, weight, body mass index, medications at randomization, pertinent medical/family/social history, i.e., hypertension, hypercholesterolemia, diabetes mellitus, current tobacco use, history of prior myocardial infarction, PCI or CABG. This data will be gathered by research coordinator through interviewing patient and checking patient's medical record.

Procedural: Exact time of onset of ischemic symptoms, of admission, of randomization, and of undertake coronary angiography will be noted by a supplemental chart, along with important information like the evidence of occurrence of an endpoint. Blood concentration of hemoglobin, BNP/NT-proBNP, creatinine, cardiac troponin and C-reaction protein will be tested at admission. First electrocardiography and echocardiography will be recorded. Thrombolysis In Myocardial Infarction flow will be recorded before and after PCI procedure, and the images will be copied to calculate the SYNTAX score afterwards.

After hospital discharge, the research coordinator will contact the patient at specified intervals （30 days after discharge, 180 days and 365 days after randomization） to determine if an endpoint has been met.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 696
• Est. completion date: October 30, 2019
• Est. primary completion date: October 30, 2019
• Accepts healthy volunteers: No
• Gender: All
• Age group: 75 Years and older

Eligibility

Inclusion Criteria:

1. Aged 75 years or older

2. Elevated cardiac troponin;

3. Ischemic symptom or ST-segment depression in ECG;

4. Newly onset of myocardial ischemia within 24 hours;

5. Written Informed Consent obtained.

Exclusion Criteria:

1. Type 2 MI (secondary to tachyarrhythmias, uncontrolled hypertension, anemia, hyperthyroidism, acute pulmonary infection, or fever)

2. Secondary elevation of cardiac troponin (e.g. renal insufficiency, heart failure, et al.)

3. Persistent ST-segment elevation or new pathologic Q wave indicating STEMI

4. Ongoing myocardial ischemia despite intensive medical treatment after admission

5. Refractory acute heart failure that can not be well controlled despite treatment for 24 hours

6. Hemodynamic instability or cardiac shock on admission

7. History of cardiac arrest or ventricular tachycardia/fibrillation after symptom onset

8. Concomitant use of oral anticoagulants for atrial fibrillation or thromboembolism diseases

9. PCI or bypass surgery within 30 days before randomization

10. History of contrast agent allergy

11. Baseline serum creatinine of >2.5 mg/dl or calculated creatinine clearance rate of <30 ml/min

12. Known bleeding diathesis or contraindications to dual antiplatelet treatment like active internal bleeding

13. Gastrointestinal and genitourinary bleeding of clinical significance within 6 weeks before randomization

14. History of stroke within 3 months

15. infectious diseases or fever

16. Life expectancy < 6 months

Related Conditions & MeSH terms

• Infarction
• Myocardial Infarction
• Non-ST Elevation Myocardial Infarction

Intervention

Procedure:
• early coronary angiography
Routine coronary angiography and revascularization if appropriate within 24 hours
• delayed coronary angiography
Routine coronary angiography and revascularization if appropriate after 72 hours

Locations

Country	Name	City	State
China	Fuwai Hospital	Beijing	Beijing

Sponsors (1)

Lead Sponsor	Collaborator
Chinese Academy of Medical Sciences, Fuwai Hospital

Country where clinical trial is conducted

China, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Composite endpoint of all-cause mortality, non-lethal myocardial infarction, stroke and urgent revascularization		1 year
Secondary	No reflow	composite and Individual component	during PCI
Secondary	All-cause mortality	composite and Individual component	30 days after discharge, 6 months and 1 year after randomization
Secondary	Non-lethal myocardial infarction	composite and Individual component	30 days after discharge, 6 months and 1 year after randomization
Secondary	Severe recurrent ischemia	composite and Individual component	30 days after discharge, 6 months and 1 year after randomization
Secondary	Stroke	composite and Individual component	30 days after discharge, 6 months and 1 year after randomization
Secondary	Major bleeding	composite and Individual component	30 days after discharge, 6 months and 1 year after randomization