Coronary Artery Disease
Conditions
Brief summary
Peri-procedural inflammation is associated with increased rates of post-procedural myocardial infarction (MI), which occur in up to 35% of PCI patients and are themselves associated with increased risk of later MI and death. Statins suppress both inflammatory markers and MI rates during and after PCI, but ≥ 40% of PCI patients go statin-untreated, due in part to side effects such as myalgia. Moreover, because their mechanism of action relies on post-translational effects, statins must be given ≥ 12 to 24 hours prior to PCI, a time frame that is not always feasible. The investigators propose a novel alternative approach to reduce inflammation during PCI employing colchicine, an anti-inflammatory medication used frequently in gout and pericarditis. Colchicine may be particularly applicable to the PCI setting due to its rapid onset of action and excellent side-effect profile at low doses, as well as its known mechanisms of action. However, data on colchicine use in patients with coronary disease is extremely limited, and no studies to date have evaluated the use of colchicine in patients undergoing PCI. The investigators aim to characterize a potential mechanism of benefit in patients undergoing PCI by evaluating the effects of colchicine on soluble and leukocyte surface markers after PCI. The investigators also aim to determine the effects of colchicine on peri-procedural myonecrosis and MI. Accordingly, the investigators propose a prospective randomized study to characterize the effect of colchicine on inflammation and peri-procedural myocnecrosis. Patients referred for possible PCI will be randomized in a double-blinded fashion to placebo or colchicine (1.2mg 1 to 2 hours before PCI, followed by 0.6mg 1 hour later). The primary endpoint will be post-procedural interleukin-6 level. Secondary endpoints will include other relevant soluble and leukocyte-associated inflammatory markers. Sample size needed is 200 patients undergoing PCI. To adjust for a floor effect, 280 patients undergoing PCI will be needed. 400 patients will likely be needed to be enrolled to reach 280 PCIs (the remaining will have undergone a diagnostic only procedure). Of note, this is a substudy of the COLCHICINE-PCI trial (NCT 02594111)
Interventions
Colchicine 1.2mg 1 to 2 hours prior PCI, followed by 0.6mg 1 hour later
Placebo 1 to 2 hours prior PCI, followed by Placebo 1 hour later
Sponsors
Study design
Eligibility
Inclusion criteria
* Patients must be more than 18 years of age and referred for coronary angiography
Exclusion criteria
* Plan for diagnostic-only coronary angiography * On colchicine chronically * History of intolerance to colchicine * Glomerular filtration rate \<30mL/minute or on dialysis * Active malignancy or infection * History of myelodysplasia * High-dose statin load \<24 hours prior to procedure * Use of oral steroids or non-steroidal anti-inflammatory agents other than aspirin within 72 hours or 3 times the agent's half-life (whichever is longer) * Use of strong CYP3A4/P-glycoprotein inhibitors (specifically ritonavir, ketoconazole, clarithromycin, cyclosporine, diltiazem and verapamil) * Unable to consent * Participating in a competing study
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Percent Change in Post-procedural IL-6 Concentration From Baseline to 30 Min -1 hr After PCI | 30 minutes to 1 hour after PCI |
Secondary
| Measure | Time frame |
|---|---|
| Percent Change in Post-procedural IL-6 Concentration From Baseline to 22-24 hr After PCI | baseline to 22-24 hr after PCI |
| Percent Change in Post-procedural hsCRP Concentration From Baseline to 22-24 hr After PCI | baseline to 22-24 hr after PCI |
| Percent Change in Post-procedural IL-1B Concentration From Baseline to 30 Min -1 hr After PCI | 30 minutes to 1 hour after PCI |
Countries
United States
Participant flow
Participants by arm
| Arm | Count |
|---|---|
| Colchicine Colchicine | 141 |
| Placebo Placebo | 139 |
| Total | 280 |
Baseline characteristics
| Characteristic | Placebo | Total | Colchicine |
|---|---|---|---|
| Age, Continuous | 65.15 years STANDARD_DEVIATION 10.38 | 64.7 years STANDARD_DEVIATION 9.8 | 64.31 years STANDARD_DEVIATION 9.29 |
| Ethnicity (NIH/OMB) Hispanic or Latino | 30 Participants | 64 Participants | 34 Participants |
| Ethnicity (NIH/OMB) Not Hispanic or Latino | 109 Participants | 216 Participants | 107 Participants |
| Ethnicity (NIH/OMB) Unknown or Not Reported | 0 Participants | 0 Participants | 0 Participants |
| Race (NIH/OMB) American Indian or Alaska Native | 0 Participants | 0 Participants | 0 Participants |
| Race (NIH/OMB) Asian | 11 Participants | 15 Participants | 4 Participants |
| Race (NIH/OMB) Black or African American | 25 Participants | 57 Participants | 32 Participants |
| Race (NIH/OMB) More than one race | 0 Participants | 0 Participants | 0 Participants |
| Race (NIH/OMB) Native Hawaiian or Other Pacific Islander | 0 Participants | 0 Participants | 0 Participants |
| Race (NIH/OMB) Unknown or Not Reported | 1 Participants | 1 Participants | 0 Participants |
| Race (NIH/OMB) White | 102 Participants | 207 Participants | 105 Participants |
| Region of Enrollment United States | 139 participants | 280 participants | 141 participants |
| Sex: Female, Male Female | 12 Participants | 23 Participants | 11 Participants |
| Sex: Female, Male Male | 127 Participants | 257 Participants | 130 Participants |
Adverse events
| Event type | EG000 affected / at risk | EG001 affected / at risk |
|---|---|---|
| deaths Total, all-cause mortality | 0 / 141 | 0 / 139 |
| other Total, other adverse events | 0 / 141 | 0 / 139 |
| serious Total, serious adverse events | 2 / 141 | 6 / 139 |
Outcome results
Percent Change in Post-procedural IL-6 Concentration From Baseline to 30 Min -1 hr After PCI
Time frame: 30 minutes to 1 hour after PCI
| Arm | Measure | Value (MEDIAN) |
|---|---|---|
| Colchicine | Percent Change in Post-procedural IL-6 Concentration From Baseline to 30 Min -1 hr After PCI | 0 % change |
| Placebo | Percent Change in Post-procedural IL-6 Concentration From Baseline to 30 Min -1 hr After PCI | 20 % change |
Percent Change in Post-procedural hsCRP Concentration From Baseline to 22-24 hr After PCI
Time frame: baseline to 22-24 hr after PCI
| Arm | Measure | Value (MEDIAN) |
|---|---|---|
| Colchicine | Percent Change in Post-procedural hsCRP Concentration From Baseline to 22-24 hr After PCI | 11 % change |
| Placebo | Percent Change in Post-procedural hsCRP Concentration From Baseline to 22-24 hr After PCI | 66 % change |
Percent Change in Post-procedural IL-1B Concentration From Baseline to 30 Min -1 hr After PCI
Time frame: 30 minutes to 1 hour after PCI
| Arm | Measure | Value (MEDIAN) |
|---|---|---|
| Colchicine | Percent Change in Post-procedural IL-1B Concentration From Baseline to 30 Min -1 hr After PCI | 0 % change |
| Placebo | Percent Change in Post-procedural IL-1B Concentration From Baseline to 30 Min -1 hr After PCI | 0 % change |
Percent Change in Post-procedural IL-1B Concentration From Baseline to 30 Min -1 hr After PCI
Time frame: baseline to 22-24 hr after PCI
| Arm | Measure | Value (MEDIAN) |
|---|---|---|
| Colchicine | Percent Change in Post-procedural IL-1B Concentration From Baseline to 30 Min -1 hr After PCI | 0 % change |
| Placebo | Percent Change in Post-procedural IL-1B Concentration From Baseline to 30 Min -1 hr After PCI | 0 % change |
Percent Change in Post-procedural IL-6 Concentration From Baseline to 22-24 hr After PCI
Time frame: baseline to 22-24 hr after PCI
| Arm | Measure | Value (MEDIAN) |
|---|---|---|
| Colchicine | Percent Change in Post-procedural IL-6 Concentration From Baseline to 22-24 hr After PCI | 76 % change |
| Placebo | Percent Change in Post-procedural IL-6 Concentration From Baseline to 22-24 hr After PCI | 338 % change |