跳至主要内容
临床试验/NCT05801289
NCT05801289招募中不适用

Quetiapine as a Prophylactic Agent for Early Postoperative Delirium in High Risk Patients in Open Heart Surgeries

Ain Shams University1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2022年12月4日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
招募中
入组人数
60
试验地点
1
主要终点
delirium incidence

研究概览

简要总结

low-dose quetiapine may be effective in preventing delirium in patients. The purpose of this study is to evaluate the efficacy and safety of quetiapine for delirium prophylaxis in cabg

详细描述

Group Q: will receive 25 mg quetiapine at night of surgery and 25 mg daily for 7 days postoperative (30 patients).

Group C: will receive placebo alone (30 patients). During the study period, enrolled patients will be assessed for delirium once daily (from 7:00 AM to 7:00 PM), and the assessment will be performed in two steps. First, level of sedation will be assessed using the RASS. If the patient will be deeply sedated or unarousable (RASS -4 or -5), the assessment will not be performed and the patient will be reassessed at a later time. If the patient has a RASS of -3to +4, then the assessment will be continued to the next step.

Second, delirium will be diagnosed using the CAM-ICU. The screening tool detects four features of delirium: acute onset of mental status change or a fluctuating course, inattention, disorganized thinking, and altered level of consciousness. To have delirium diagnosed, a patient displays the first two features with either the third or fourth feature.

The primary outcome is delirium incidence diagnosed with the CAM_ICU within the study period. If the CAM_ICU is positive at least once during the study period, it will be recorded that a delirium occurred.

Secondary outcomes is the rate of positive CAM-ICU (the number of positive CAM-ICU counts/the number of total CAM-ICU counts), days without delirium (number of days from the start of treatment until delirium), the duration of delirium if it appear (number of days with delirium), severity of delirium as measured with delirium rating scale revised 98 (DRS-R-89), the length of stay in the ICU, the length of stay in the hospital, the duration of intubation, a successful extubation, the ICU mortality, the overall mortality, measurement of QTc prolongation, and the use of rescue medication.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
None

入排标准

年龄范围
65 Years 至 —(Older Adult)
性别
All
接受健康志愿者

入选标准

  • Patients aged 65 or older old of age undergoing open heart surgery and having an equal or greater score of 5 on the scale of Delphi.
  • Age: 70-79 years: 1 point; ≥ 80 years: 2 points
  • Physical activity: need for assistance, not self-sufficient: 2 points
  • Alcoholism: 1 point
  • Hearing impaired: 1 point
  • History of delirium: 2 points
  • Emergency of surgery: 2 points
  • No laparoscopic surgery: 2 points
  • Admission critical unites: 3 points
  • Value of C reactive protein (CRP) ≥ 10mg/dl: 1 point

排除标准

  • .Patient refusal.
  • Allergy to quetiapine
  • Patients with a score less than 5 on Delphi scale
  • Diagnosis of delirium on admission initial CAM-ICU (the Confusion Assessment Method-ICU) positive)
  • Could not communicate due to previously diagnosed irreversible neurologic disease (stroke, cerebral hemorrhage, traumatic brain injury, dementia, etc.)
  • High risk for ventricular arrhythmias (Corrected QT interval ≥ 460 millisecond in men, ≥ 470 millisecond in women or ongoing treatment with drugs known to prolong the QT interval (e.g., erythromycin, class Ia, Ic, III anti-arrhythmic drugs)
  • Second or third degree heart block
  • High risk for drug interaction with quetiapine (phenytoin, carbamazepine, barbiturates)
  • Electrolyte disturbance : Potassium less than 3 or magnesium less than 1.5
  • Patient on antipsychotic drug treatment prior to admission
  • Parkinson's disease

研究组 & 干预措施

Group Q

Active Comparator

will receive 25 mg quetiapine at night of surgery and 25 mg daily for 7 days postoperative

干预措施: Quetiapine (Drug)

结局指标

主要结局

delirium incidence

时间窗: 3 days postoperative

CAM_ICU

次要结局

  • severity of delirium(7 days postoperative)
  • length of stay in the ICU(3 days postoperative)
  • duration of delirium if it appear(7 days postoperative)
  • days without delirium(5 days postoperative)
  • the length of stay in the hospital(7 days postoperative)
  • the ICU mortality(3 days postoperative)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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