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NCT Number: NCT01709981

Anti-inflammatory Effects of Colchicine in PCI

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)

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 4

Primary location

Bellevue Hospital Center, New York, United States

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Who can participate

Healthy volunteers accepted: No

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

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

Treatment and study plan

Colchicine

Drug

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

Other names: Colcrys

Placebo

Drug

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

Primary outcomes

  1. 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

Secondary outcomes

  1. 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

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

    Time frame: baseline to 22-24 hr after PCI

  3. 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

  4. 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

Sponsors and collaborators

Lead sponsor

NYU Langone Health

Other

Collaborators

  • Takeda

Registry information

Official study title

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

Important dates

Study start
2013
Primary completion
2019
Study completion
2021
First posted
Oct 18, 2012
Registry last updated
May 25, 2022

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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