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COlchicine in Cardiac Surgery (COCS)

Primary Purpose

Colchicine Adverse Reaction, Atrial Fibrillation New Onset

Status
Completed
Phase
Phase 4
Locations
Russian Federation
Study Type
Interventional
Intervention
Colchicine Pill
Placebo
Sponsored by
Bakulev Scientific Center of Cardiovascular Surgery
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Colchicine Adverse Reaction focused on measuring Colchicine, Postoperative atrial fibrillation, Anti-inflammatory, Cardiac surgery, Sympatholytic

Eligibility Criteria

40 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

Adult patients awaiting elective cardiac surgery (CABG and/or AVR (aortic valve replacement), who are willing and able to give informed consent for participation in the study and who are in sinus rhythm and not taking any antiarrhythmic medication, except beta-adrenergic blocking agents, at the time before surgery.

Exclusion Criteria:

  • History of persistent or long-term atrial fibrillation/atrial flutter
  • Congenital heart disease, except the bicuspid AV
  • Frequent VE/SVE, AV block 2-3 degrees
  • Use of corticosteroids during the last month
  • Taking any antiarrhythmic drugs, except beta-blockers, within the last 1 month
  • Prior "open" heart surgery
  • Moderate to severe renal failure (creatinine clearance < 50 ml / min)
  • History of obstructive hepato-biliary disease or other serious hepatic disease
  • Significant mitral valve disease (moderate or severe mitral regurgitation-eg. > grade II and/or mitral stenosis & mitral annular calcification).
  • Patient participation in another clinical trial

Sites / Locations

  • Federal Center for Cardiovascular Surgery (Astrakhan)
  • Bakulev National Medical Research Center for Cardiovascular Surgery

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

Colchicine

Placebo

Arm Description

Colchicine 1 mg day (COLCHICINA LIRCA ® ACARPIA Farmaceutici S.r.l.)

Sugar pill

Outcomes

Primary Outcome Measures

Number of participants with postoperative atrial fibrillation.
POAF detected on continuous ECG monitoring.

Secondary Outcome Measures

Number of participants with lethal and non-lethal events.
The main nosocomial lethal and non-lethal events (death, stroke, myocardial infarction, heart failure).
Fluid in the pericardium.
Fluid in the pericardium evaluated by echocardiography.
Fluid in the pleura.
Fluid in the pleura evaluated by echocardiography.
Acute kidney damage (according to the dynamics of creatinine clearance).
Dynamics of creatinine clearance.
Inflammation in blood plasma.
Dynamics of biomarker of inflammation in blood plasma (neutrophils).
Liver damage
Dynamics of biomarkers of liver damage (aspartate aminotransferase, alanine aminotransferase).

Full Information

First Posted
December 27, 2019
Last Updated
November 9, 2022
Sponsor
Bakulev Scientific Center of Cardiovascular Surgery
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1. Study Identification

Unique Protocol Identification Number
NCT04224545
Brief Title
COlchicine in Cardiac Surgery
Acronym
COCS
Official Title
Colchicine for Prevention Atrial Fibrillation After Cardiac Surgery in the Early Postoperative Period
Study Type
Interventional

2. Study Status

Record Verification Date
August 2022
Overall Recruitment Status
Completed
Study Start Date
December 23, 2019 (Actual)
Primary Completion Date
August 15, 2022 (Actual)
Study Completion Date
August 23, 2022 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Bakulev Scientific Center of Cardiovascular Surgery

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Postoperative atrial fibrillation (POAF) is a major complication of cardiac surgery, which could lead to high morbidity and mortality, increase duration of hospital stay and increase the cost of treatment. Colchicine possesses both anti-inflammatory and sympatholytic properties, so it has been studied to prevent POAF. The ACC/AHA guidelines for colchicine contain a class IIB recommendation, but the ESC guidelines do not recommend this drug. More researches are needed to focus on reducing of side effects by optimizing the colchicine regimen to reduce the incidence of gastrointestinal side effects. It is believed that further research is needed to investigate the efficacy and safety of colchicine in these conditions. This research is aimed to study the effectiveness of short-term administration of the drug.
Detailed Description
Postoperative atrial fibrillation (POAF) is a major complication of cardiac surgery, which could lead to high morbidity and mortality, increase duration of hospital stay and increase the cost of treatment. Postoperative AF is considered as a multifactorial phenomenon. Its pathogenesis is characterized by inflammation, oxidative stress and autonomic dysfunction. Several predisposing factors lead to the development of POAF, including pre -, intra-and postoperative factors. The main of them are age, previous history of major cardiovascular risk factors and ischemic reperfusion injury during surgery. Treatment of POAF involves drugs to control the frequency of rhythm in hemodynamically stable patients and other treatment regimens usually used for the treatment of AF. Intraoperative administration of beta-blockers and some antiarrhythmic drugs is recommended by international clinical guidelines. In addition, previous treatment consisting of the use of colchicine, magnesium sulfate, statins and antioxidants have reduced the incidence of postoperative AF. However, the results of large-scale randomized trials have observed the development of undesirable adverse reactions. Despite these recommendations, the question of the correct regimen for prevention of POAF remains controversial. Colchicine possesses both anti-inflammatory and sympatholytic properties, so it has been studied to prevent POAF. The ACC/AHA guidelines for colchicine contain a class IIB recommendation, but the ESC guidelines do not recommend this drug. Two studies sequentially COPPS-1 and COPPS-2 evaluated the effect of colchicine on the incidence of POAF after open heart surgery (COPPS-1) and the development of postcardiotomy syndrome (COPPS-2). In COPPS-1, patients (n=336) were treated with colchicine from the third day after surgery for a month and showed a significant decrease of POAF after heart surgery over the entire follow-up period. 360 patients were evaluated in the COPPS-2 study. The incidence of POAF between the colchicine and placebo groups was comparable, although colchicine significantly reduced postpericardiotomy syndrome. The main limitation of the COPSS-2 study was the high rate of cessation of intervention (20% of participants), which had a significant impact on the outcome of the trial. Based on the latest meta-analysis of the colchicine effect on POAF after heart surgery, it was found that it still reduces POAF compared with control (HR = 0.69, 95% IM 0.57-0.84, p = 0.0002) and the duration of hospital stay was reduced by 1.2 days (95% IM -1.89 to -0.44, p = 0.002); however, the frequency of adverse gastrointestinal events increased significantly (HR = 2.52, 95% IM 1.62-3.93, p < 0.0001). Despite the high level of side effects, a significant reduction of POAF outweighs the balance in the favor of its use. However, more researches are needed to focus on reducing of side effects by optimizing the colchicine regimen to reduce the incidence of gastrointestinal side effects. It is believed that further research is needed to investigate the efficacy and safety of colchicine in these conditions. This research is aimed to study the effectiveness of short-term administration of the drug.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Colchicine Adverse Reaction, Atrial Fibrillation New Onset
Keywords
Colchicine, Postoperative atrial fibrillation, Anti-inflammatory, Cardiac surgery, Sympatholytic

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Model Description
A randomized double-blind controlled trial in two groups
Masking
ParticipantCare ProviderInvestigator
Allocation
Randomized
Enrollment
267 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Colchicine
Arm Type
Experimental
Arm Description
Colchicine 1 mg day (COLCHICINA LIRCA ® ACARPIA Farmaceutici S.r.l.)
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Sugar pill
Intervention Type
Drug
Intervention Name(s)
Colchicine Pill
Other Intervention Name(s)
group C
Intervention Description
Colchicine at a dose of 1 mg a day before surgery, 2, 3, 4, 5 days after surgery.
Intervention Type
Drug
Intervention Name(s)
Placebo
Other Intervention Name(s)
group P
Intervention Description
Placebo started a day before surgery, 2, 3, 4, 5 days after surgery.
Primary Outcome Measure Information:
Title
Number of participants with postoperative atrial fibrillation.
Description
POAF detected on continuous ECG monitoring.
Time Frame
Monitoring is carried out immediately after surgery and will be continued until the end of the 7th postoperative day.
Secondary Outcome Measure Information:
Title
Number of participants with lethal and non-lethal events.
Description
The main nosocomial lethal and non-lethal events (death, stroke, myocardial infarction, heart failure).
Time Frame
Participants will be followed for the duration of the postoperative period up to the day of initial discharge from the hospital, an expected average of 7 days.
Title
Fluid in the pericardium.
Description
Fluid in the pericardium evaluated by echocardiography.
Time Frame
Diagnostics will be carried out on the 3rd and 5th day after surgery.
Title
Fluid in the pleura.
Description
Fluid in the pleura evaluated by echocardiography.
Time Frame
Diagnostics will be carried out on the 3rd and 5th day after surgery.
Title
Acute kidney damage (according to the dynamics of creatinine clearance).
Description
Dynamics of creatinine clearance.
Time Frame
Diagnostics will be carried out a day before surgery and on the 3rd and 5th day after surgery.
Title
Inflammation in blood plasma.
Description
Dynamics of biomarker of inflammation in blood plasma (neutrophils).
Time Frame
Diagnostics will be carried out a day before surgery and on the 3rd and 5th day after surgery.
Title
Liver damage
Description
Dynamics of biomarkers of liver damage (aspartate aminotransferase, alanine aminotransferase).
Time Frame
Diagnostics will be carried out a day before surgery and on the 3rd and 5th day after surgery.

10. Eligibility

Sex
All
Minimum Age & Unit of Time
40 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Adult patients awaiting elective cardiac surgery (CABG and/or AVR (aortic valve replacement), who are willing and able to give informed consent for participation in the study and who are in sinus rhythm and not taking any antiarrhythmic medication, except beta-adrenergic blocking agents, at the time before surgery. Exclusion Criteria: History of persistent or long-term atrial fibrillation/atrial flutter Congenital heart disease, except the bicuspid AV Frequent VE/SVE, AV block 2-3 degrees Use of corticosteroids during the last month Taking any antiarrhythmic drugs, except beta-blockers, within the last 1 month Prior "open" heart surgery Moderate to severe renal failure (creatinine clearance < 50 ml / min) History of obstructive hepato-biliary disease or other serious hepatic disease Significant mitral valve disease (moderate or severe mitral regurgitation-eg. > grade II and/or mitral stenosis & mitral annular calcification). Patient participation in another clinical trial
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Vladimir Shvartz
Organizational Affiliation
Bakulev National Medical Research Center for Cardiovascular Surgery
Official's Role
Principal Investigator
Facility Information:
Facility Name
Federal Center for Cardiovascular Surgery (Astrakhan)
City
Astrakhan
Country
Russian Federation
Facility Name
Bakulev National Medical Research Center for Cardiovascular Surgery
City
Moscow
Country
Russian Federation

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
The datasets analyzed during the current study are publicly available. The data is available in the general repository "Open Science Framework" at the link
IPD Sharing Time Frame
until 2045
IPD Sharing Access Criteria
open access
IPD Sharing URL
https://doi.org/10.17605/OSF.IO/HPCZW
Citations:
PubMed Identifier
35268478
Citation
Shvartz V, Le T, Kryukov Y, Sokolskaya M, Ispiryan A, Khugaeva E, Yurkulieva G, Shvartz E, Petrosyan A, Bockeria L, Bockeria O. Colchicine for Prevention of Atrial Fibrillation after Cardiac Surgery in the Early Postoperative Period. J Clin Med. 2022 Mar 3;11(5):1387. doi: 10.3390/jcm11051387.
Results Reference
result
PubMed Identifier
36286314
Citation
Shvartz V, Le T, Enginoev S, Sokolskaya M, Ispiryan A, Shvartz E, Nudel D, Araslanova N, Petrosyan A, Donakanyan S, Chernov I, Bockeria L, Golukhova E. Colchicine in Cardiac Surgery: The COCS Randomized Clinical Trial. J Cardiovasc Dev Dis. 2022 Oct 20;9(10):363. doi: 10.3390/jcdd9100363.
Results Reference
result
Available IPD and Supporting Information:
Available IPD/Information Type
Individual Participant Data Set
Available IPD/Information URL
https://doi.org/10.17605/OSF.IO/HPCZW
Available IPD/Information Comments
The datasets analyzed during the current study are publicly available. The data is available in the general repository "Open Science Framework" at the link

Learn more about this trial

COlchicine in Cardiac Surgery

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