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临床试验/NCT06118034
NCT06118034招募中3 期

Effect of Colchicine on Perioperative Anti-inflammatory Organ Injury in Cardiac Surgery : a Multi-center, Randomized, Controlled, Double-blind Clinical Trial

The Affiliated Nanjing Drum Tower Hospital of Nanjing University Medical School1 个研究点 分布在 1 个国家目标入组 768 人开始时间: 2024年1月28日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
3 期
状态
招募中
发起方
入组人数
768
试验地点
1
主要终点
Number of Participants with POAF

研究概览

简要总结

All patients will be completed collection of demographic data, clinical data, and be observed for inflammatory organ damage, oxygenation index or SpO2/ FIO2, WBC, NEU, interleukin-1β, interleukin-6, interleukin-8 (IL-1β/6/8), tumor necrosis factor-α (TNF-α), C-reactive protein (CRP), procalcitonin (PCT), myoglobin (Myo), creatine kinase-MB (CK-MB), high-sensitivity cardiac troponin T (hs-cTnT), neutrophil elastase (NE), myeloperoxidase (MPO), APACHE II score, alanine transaminase (ALT), aspartate transaminase (AST), total bilirubin, Murray lung injury score, serum creatinine, eGFR, mechanical ventilation time, ICU length of stay, drug-related gastrointestinal reactions, and 30-day and 90-day all-cause mortality, among other indicators.

详细描述

This study is a multicenter, randomized, controlled, double-blind, placebo- controlled clinical trial. A total of 768 patients who met the inclusion and exclusion criteria and were scheduled for cardiac surgery under cardiopulmonary bypass were enrolled. After signing informed consent, patients were randomly divided into the experimental group and the control group. Patients in the experimental group took 0.5mg of colchicine tablets orally for 3 days before surgery and continued to take 0.5mg daily for 10 days after tracheal extubation. Patients in the control group received an equivalent amount of starch placebo tablets, administered at the same times and in the same doses as the experimental group, during the colchicine/placebo treatment period, without affecting the patients' standard treatment protocols.

All patients will be completed collection of demographic data, clinical data, and be observed for inflammatory organ damage, oxygenation index or SpO2/ FIO2, WBC, NEU, interleukin-1β, interleukin-6, interleukin-8 (IL-1β/6/8), tumor necrosis factor-α (TNF-α), C-reactive protein (CRP), procalcitonin (PCT), myoglobin (Myo), creatine kinase-MB (CK-MB), high-sensitivity cardiac troponin T (hs-cTnT), neutrophil elastase (NE), myeloperoxidase (MPO), APACHE II score, alanine transaminase (ALT), aspartate transaminase (AST), total bilirubin, Murray lung injury score, serum creatinine, eGFR, mechanical ventilation time, ICU length of stay, drug-related gastrointestinal reactions, and 30-day and 90-day all-cause mortality, among other indicators. The study aims to investigate the impact of colchicine on the levels of inflammatory factors and prognosis in patients undergoing cardiac vascular surgery and to observe the potential organ damage to the heart, lungs, liver, kidneys, and the occurrence of adverse events such as leukopenia and thrombocytopenia. This is done to assess the safety of colchicine use in cardiac surgery patients.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Triple (Participant, Investigator, Outcomes Assessor)

入排标准

年龄范围
50 Years 至 80 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • 未提供

排除标准

  • 未提供

研究组 & 干预措施

Experimental group (colchicine group)

Experimental

The experimental group take 0.5mg of colchicine tablets orally for 3 days before surgery, and continue to take 0.5mg every other day (qod) for 10 days after tracheal extubation.

干预措施: Colchicine 0.5 MG (Drug)

Control group

Placebo Comparator

The control group take 0.5mg of placebo tablets orally for 3 days before surgery, and continue to take 0.5mg every other day (qod) for 10 days after tracheal extubation.

干预措施: Placebo (Drug)

结局指标

主要结局

Number of Participants with POAF

时间窗: postoperative 10 days

POAF: Onset of new atrial fibrillation in patients within 10 days post-surgery.

Number of Participants with PMI

时间窗: postoperative 10 days

PMI: Patient's high-sensitivity cardiac troponin T (hs-cTnT) exceeds 0.8 ng/L on the first day after surgery, and there is an increase of 10% or more on the second day compared to the first day postoperatively.

Number of Participants with ARDS

时间窗: postoperative 10 days

ARDS: Acute Respiratory Distress Syndrome

Number of Participants with PPS

时间窗: postoperative 10 days

PPS: post-pericardiotomy syndrome

次要结局

  • Myocardial injury marker(postoperative day 1, 3, 5 and 7)
  • blood transfusion(Surgical day)
  • Rate of exudates on chest radiograph(postoperative 14 days)
  • Oxygenation index(postoperative day 1, 3, 5 and 7)
  • Inflammatory index(postoperative day 1, 3, 5 and 7)
  • Acute physiology and chronic health evaluation(APACHE II) socre(postoperative day 1, 3, 5 and 7)
  • Murray lung injury score(postoperative day 1, 3, 5 and 7)
  • Liver and kidney function(postoperative day 1, 3, 5 and 7)
  • DVMV(postoperative 28 days)
  • ICU time(postoperative 28 days)
  • In-hospital time(postoperative 28 days)
  • 30-day all-cause mortality(postoperative 30 days)
  • 90-day all-cause mortality(postoperative 90 days)
  • Incidence of gastrointestinal reactions(postoperative 7 days)
  • Surgical data(Surgical day)

研究者

发起方
The Affiliated Nanjing Drum Tower Hospital of Nanjing University Medical School
申办方类型
Other
责任方
Sponsor

研究点 (1)

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