COlchicine for Left VEntricular Remodeling Treatment in Acute Myocardial Infarction

Phase 2

Completed

• Conditions: Myocardial Infarction
• Interventions: Drug: Colchicine group (experimental arm); Drug: Placebo group (control arm)

• Registration Number: NCT03156816
• Lead Sponsor: Hospices Civils de Lyon

Brief Summary

Inflammatory processes have been identified as key mediators of ischemia/ reperfusion injury in ST-segment elevation myocardial infarction. They add additional damage to the myocardium and are associated with clinical adverse events (heart failure and cardiovascular death) and poor myocardial recovery. All the different anti-inflammatory approaches to reduce reperfusion injury have been disappointing.

Colchicine is a well-known substance with potent anti-inflammatory properties. In a recent pilot study performed in 151 acute STEMI patients treated with primary percutaneous coronary intervention(PPCI) Deftereos et al. showed a 50% reduction of infarct size (creatine kinase release) with a short course treatment of colchicine in comparison to placebo.

One mechanism to explain this effect could be the reduction of adverse left ventricular (LV) remodelling. LV remodelling is part of the healing process of myocardium after MI. It is defined as the end diastolic volume (EDV) increase in the first months after MI. Adverse LV remodelling is increased by inflammation and ultimately leads to heart failure.

Our main hypothesis is that colchicine with its anti-inflammatory properties significantly reduces the initiation of adverse LV remodelling, together with a significant reduction of infarct size and microvascular obstruction in comparison to placebo in acute STEMI patients referred for PPCI.

After inclusion and randomisation, patients will receive the first part of their experimental treatment: colchicine or placebo before PCI, then, the second part after PCI and during 5 days. They will be followed up during their hospitalization and until one year. In order to evaluate LV remodelling, two cardiac magnetic resonance studies will be performed during their participation: one during their hospitalization and a second at 3 months. At 1 year, adverse events will be collected by phone.

Detailed Description

Not available

Study Timeline

• Study First Submitted: 2017-05-16
• Study First Submitted QC: 2017-05-16
• Study First Posted: 2017-05-17
• Study Start: 2018-07-23
• Primary Completion: 2020-11-08
• Study Completion: 2021-08-16
• Status Verified: 2022-01
• Last Update Submitted: 2022-01-20
• Last Update Posted: 2022-01-21

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 194

Inclusion Criteria

• All patients, aged over 18 and <80 years,
• Presenting within 12 hours of chest pain onset,
• With ST segment elevation ≥ 0.2 mV in two contiguous leads or new onset of left bundle branch block,
• Referral for primary percutaneous coronary intervention (PPCI).
• Preliminary oral informed consent followed by signed informed consent as soon as possible
• With an initially occluded coronary artery (TIMI angiographic flow of the culprit coronary artery ≤1)

Read More

Exclusion Criteria

• Patients with any legal protection measure,
• Patients without any health coverage,
• Patients with loss of consciousness or confused
• Patients with a history of prior myocardial infarction
• Patients with cardiogenic shock as defined by a systolic blood pressure <90 mmHg, despite 30 minutes of fluid challenge or requiring intravenous vasoactive agents (dobutamine, noradrenaline, adrenaline)
• Patient with severe liver or known renal dysfunction (known GFR≤30 ml/min)
• Patient with known history of severe drug intolerance to colchicine
• Female patients currently pregnant or women of childbearing age not using contraception (oral diagnosis)
• Patients with any obvious contraindication to magnetic resonance imaging (claustrophobia, pace maker, defibrillator....)
• Patients treated by macrolides or pristinamycin
• Chronic treatment with COLCHICINE (Mediterranean familial fever mainly)
• Patient with lactose intolerance
• Patient with swallowing disorders

Read More

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Colchicine	Colchicine group (experimental arm)	The patients will receive an oral bolus of colchicine of 2 mg followed by 0.5 mg b.i.d. during 5 days.
Control arm	Placebo group (control arm)	The patients will receive an oral bolus of placebo of 2 mg followed by 0.5 mg b.i.d. during 5 days.

Primary Outcome Measures

Name	Time	Method
infarct size (in % of LV mass) as estimated by CMR	5 days	The primary endpoint will be the infarct size as estimated by CMR at 5 days follow-up between both groups

Secondary Outcome Measures

Name	Time	Method
LV ejection fraction	At 5 days
Relative ventricular remodeling (%)	at 3 months
LVEDV	At 3 months	LVEDV (indexed to body surface area) as determined by CMR at the acute phase and 3 months follow-up respectively
LVESV	at 3 months	LVEDV (indexed to body surface area) as determined by CMR at the acute phase and 3 months follow-up respectively
Relative LV ejection fraction	5 days
Absolute adverse left ventricular remodeling (mL)	at 3 months
Infarct size in % of LV mass	At 3 months	Infarct size in % of LV mass assessed by ce-CMR
number of treatment discontinuation	5 days
Microvascular obstruction (in % of LV mass)	At 5 days
Percent of thrombi in the LV	At 5 days
Incidence of major adverse cardiovascular events	At 12 months	All cause death, cardiovascular death, heart failure worsening during initial hospitalization, hospitalization for heart failure, non-fatal myocardial infarction, life-threatening ventricular arrhythmias and atrial fibrillation.
Quality of life assessed by the EuroQol-5D (EQ5D) questionnaire	At 12 months	Evaluation of quality of life by the EQ5D questionnaire ( scale on which the best state is marked 100 and the worst state is marked 0).
number of adverse events	up to 5 days	(diarrhea, nausea/vomiting and myelotoxicity, renal function at 48H).
Dosage of inflammation biomarkers	up to 3 months	Dosage of inflammation biomarkers; * For all centers: neutrophil count, C-reactive protein, hematology, Platelets, fibrinogen.; * For the centers participating to the BioCollection: interleukin 6, interleukin 8, interleukin 1β and interleukin 18, complement system components.

Trial Locations

Locations (8)

Centre Hospitalier Universitaire Angers; 🇫🇷 Angers, France

CHRU de Tours; 🇫🇷 Tours, France

CHU Arnaud de Villeneuve; 🇫🇷 Montpellier, France

CHU de Mulhouse; 🇫🇷 Mulhouse, France

CHU de Rangueil; 🇫🇷 Toulouse, France

CHU de Poitiers; 🇫🇷 Poitiers, France

Hôpital Louis Pradel; 🇫🇷 Bron, France

Hôpital Saint Joseph; 🇫🇷 Lyon, France