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Anti-inflammatory Effects of Colchicine in PCI

Anti-inflammatory Effects of Colchicine in Patients Undergoing Percutaneous Coronary Intervention: Inflammatory Marker Substudy of the Colchicine-PCI Trial

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01709981
Enrollment
280
Registered
2012-10-18
Start date
2013-05-30
Completion date
2021-12-13
Last updated
2022-05-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Coronary Artery Disease

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

DRUGColchicine

Colchicine 1.2mg 1 to 2 hours prior PCI, followed by 0.6mg 1 hour later

DRUGPlacebo

Placebo 1 to 2 hours prior PCI, followed by Placebo 1 hour later

Sponsors

Takeda
CollaboratorINDUSTRY
NYU Langone Health
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
FACTORIAL
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

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

MeasureTime frame
Percent Change in Post-procedural IL-6 Concentration From Baseline to 30 Min -1 hr After PCI30 minutes to 1 hour after PCI

Secondary

MeasureTime frame
Percent Change in Post-procedural IL-6 Concentration From Baseline to 22-24 hr After PCIbaseline to 22-24 hr after PCI
Percent Change in Post-procedural hsCRP Concentration From Baseline to 22-24 hr After PCIbaseline to 22-24 hr after PCI
Percent Change in Post-procedural IL-1B Concentration From Baseline to 30 Min -1 hr After PCI30 minutes to 1 hour after PCI

Countries

United States

Participant flow

Participants by arm

ArmCount
Colchicine
Colchicine
141
Placebo
Placebo
139
Total280

Baseline characteristics

CharacteristicPlaceboTotalColchicine
Age, Continuous65.15 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 Participants64 Participants34 Participants
Ethnicity (NIH/OMB)
Not Hispanic or Latino
109 Participants216 Participants107 Participants
Ethnicity (NIH/OMB)
Unknown or Not Reported
0 Participants0 Participants0 Participants
Race (NIH/OMB)
American Indian or Alaska Native
0 Participants0 Participants0 Participants
Race (NIH/OMB)
Asian
11 Participants15 Participants4 Participants
Race (NIH/OMB)
Black or African American
25 Participants57 Participants32 Participants
Race (NIH/OMB)
More than one race
0 Participants0 Participants0 Participants
Race (NIH/OMB)
Native Hawaiian or Other Pacific Islander
0 Participants0 Participants0 Participants
Race (NIH/OMB)
Unknown or Not Reported
1 Participants1 Participants0 Participants
Race (NIH/OMB)
White
102 Participants207 Participants105 Participants
Region of Enrollment
United States
139 participants280 participants141 participants
Sex: Female, Male
Female
12 Participants23 Participants11 Participants
Sex: Female, Male
Male
127 Participants257 Participants130 Participants

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
deaths
Total, all-cause mortality
0 / 1410 / 139
other
Total, other adverse events
0 / 1410 / 139
serious
Total, serious adverse events
2 / 1416 / 139

Outcome results

Primary

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

ArmMeasureValue (MEDIAN)
ColchicinePercent Change in Post-procedural IL-6 Concentration From Baseline to 30 Min -1 hr After PCI0 % change
PlaceboPercent Change in Post-procedural IL-6 Concentration From Baseline to 30 Min -1 hr After PCI20 % change
p-value: 0.31Wilcoxon (Mann-Whitney)
Secondary

Percent Change in Post-procedural hsCRP Concentration From Baseline to 22-24 hr After PCI

Time frame: baseline to 22-24 hr after PCI

ArmMeasureValue (MEDIAN)
ColchicinePercent Change in Post-procedural hsCRP Concentration From Baseline to 22-24 hr After PCI11 % change
PlaceboPercent Change in Post-procedural hsCRP Concentration From Baseline to 22-24 hr After PCI66 % change
Secondary

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

ArmMeasureValue (MEDIAN)
ColchicinePercent Change in Post-procedural IL-1B Concentration From Baseline to 30 Min -1 hr After PCI0 % change
PlaceboPercent Change in Post-procedural IL-1B Concentration From Baseline to 30 Min -1 hr After PCI0 % change
Secondary

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

ArmMeasureValue (MEDIAN)
ColchicinePercent Change in Post-procedural IL-1B Concentration From Baseline to 30 Min -1 hr After PCI0 % change
PlaceboPercent Change in Post-procedural IL-1B Concentration From Baseline to 30 Min -1 hr After PCI0 % change
Secondary

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

ArmMeasureValue (MEDIAN)
ColchicinePercent Change in Post-procedural IL-6 Concentration From Baseline to 22-24 hr After PCI76 % change
PlaceboPercent Change in Post-procedural IL-6 Concentration From Baseline to 22-24 hr After PCI338 % change

Source: ClinicalTrials.gov · Data processed: Feb 18, 2026