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临床试验/NCT07466108
NCT07466108招募中不适用

Hemodynamic Effects of Intravenous Paracetamol in Patients Undergoing Emergency Laparotomy: a Randomized Controlled Trial

Cairo University1 个研究点 分布在 1 个国家目标入组 90 人开始时间: 2026年3月18日最近更新:
干预措施

试验速览

阶段
不适用
状态
招募中
入组人数
90
试验地点
1
主要终点
Mean arterial pressure

研究概览

简要总结

Emergency laparotomy is a high-risk procedure often performed in patients with severe physiological derangements due to sepsis, making perioperative management challenging. Although multimodal analgesia is essential, options are often limited by factors such as hemodynamic instability, renal dysfunction, and coagulopathy. Intravenous paracetamol is commonly recommended for perioperative analgesia because of its opioid-sparing effect, but evidence suggests it may cause hypotension through peripheral vasodilation, particularly in critically ill patients. Most data on this effect come from observational studies, and evidence regarding its intraoperative hemodynamic impact remains limited.

详细描述

Preoperative fluid administration will be guided by stroke volume change after passive leg raising maneuver Patients will receive propofol 2 mg/kg and fentanyl 1 µg/kg for induction, followed by succinylcholine 1 mg/kg for intubation. Anesthesia will be maintained with isoflurane (end-tidal 1.2%) and atracurium 0.5 mg/kg, then 0.1 mg/kg every 20 minutes.

After administration of the study drug (paracetamol or placebo), Heart rate and blood pressure will be monitored at 2 min intervals for 20 min. If patients developed hypotension (mean arterial pressure [MAP] ≤ 70% of the baseline reading and/or <65 mmHg), a 5-mcg bolus of norepinephrine will be given. The norepinephrine bolus will be repeated if mean arterial pressure was not restored within 2 min.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Other
盲法
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

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

入选标准

  • Adult patients, ASA I-III undergoing emergency laparotomy

排除标准

  • Severe cardiac morbidities (impaired contractility with ejection fraction < 40%, heart block, arrhythmias, tight valvular lesions)
  • Hemodynamically unstable patients (defined as patients with MAP < 65 mmHg or need vasopressor to maintain MAP>65 mmHg).
  • Patients with high shock index (heart rate / systolic blood pressure >1)
  • Pregnant or lactating women,
  • Allergy of any of the study drugs

研究组 & 干预措施

Paracetamol group

Active Comparator

干预措施: Paracetamol (acetaminophen) (Drug)

Control group

Placebo Comparator

干预措施: Placebo Control (Other)

结局指标

主要结局

Mean arterial pressure

时间窗: 10 minutes after infusion of the study drug

noninvasive mean arterial pressure

次要结局

  • Heart rate(from drug administration until 30 minutes after drug administration)
  • mean arterial pressure(from drug administration until 30 minutes after drug administration)
  • drug induced hypotension(from drug administration until 30 minutes after drug administration)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Ahmed Hasanin

Professor

Cairo University

研究点 (1)

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