跳至主要内容
临床试验/NCT06304181
NCT06304181尚未招募不适用

Effect of Paracetamol and Mannitol Injection on Postoperative Analgesia in Patients With Thoracoscopic Lobectomy

The Fourth Affiliated Hospital of Zhejiang University School of Medicine0 个研究点目标入组 90 人开始时间: 2024年3月15日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
90
主要终点
NRS scores

研究概览

简要总结

This study thoroughly evaluates the efficacy of acetaminophen mannitol injection for postoperative analgesia in patients undergoing thoracoscopic lobectomy, by comparing it with a control group.

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
Double (Participant, Care Provider)

入排标准

年龄范围
18 Years 至 60 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Obtain informed consent;
  • Patients scheduled for partial lobectomy under thoracoscopy with general anesthesia;
  • Classified as American Society of Anesthesiologists (ASA) physical status I~II;
  • Age over 18 years;
  • Patients voluntarily participate and sign the informed consent form

排除标准

  • Systolic blood pressure ≥180 mm Hg or <90 mm Hg, diastolic blood pressure ≥110 mm Hg or <60 mmHg
  • heart rate <50 beats/min;
  • Patients with severe liver or kidney dysfunction (severe liver dysfunction: ALT, conjugated bilirubin, AST, ALP, total bilirubin any one >2 times the upper limit of normal
  • severe kidney dysfunction: creatinine clearance <60 ml/min);
  • Patients with diabetes and complications (diabetic ketoacidosis, hyperosmolar coma, various infections, major vascular changes, diabetic nephropathy, retinopathy, diabetic cardiomyopathy, diabetic neuropathy, diabetic foot, etc.);
  • Patients with severe pulmonary impairment, such as asthma or chronic obstructive pulmonary disease;
  • History of psychiatric illness or long-term use of psychiatric drugs, chronic pain medication, or history of alcohol abuse;
  • Neuromuscular diseases;
  • Tendency towards malignant hyperthermia;
  • Allergy to the study drug or other contraindications;
  • Participation in another drug clinical trial within the past 30 days;
  • Any cerebrovascular accidents such as stroke, transient ischemic attack (TIA) in the last 3 months;
  • Unstable angina, myocardial infarction in the last 3 months;
  • Undergone another surgery within the last 3 months;
  • Coagulopathy

研究组 & 干预措施

Paracetamol and Mannitol Injection group

Experimental

Paracetamol and Mannitol Injection 500mg was given intravenously 30 minutes before the end of the operation

干预措施: Paracetamol and Mannitol Injection (Drug)

Parecoxib group

Active Comparator

40mg of parecoxib was given intravenously 30min before the end of the operation

干预措施: Parecoxib (Drug)

结局指标

主要结局

NRS scores

时间窗: after extubation 10 (±5) minutes, before leaving the resuscitation room, 6 hours, 12 hours, 24 hours after surgery

NRS scores at rest and during movement (coughing) after extubation 10 (±5) minutes, before leaving the resuscitation room, 6 hours, 12 hours, 24 hours after surgery

RASS score

时间窗: after extubation 10 (±5) minutes and 24 hours after surgery

RASS score after extubation 10 (±5) minutes and 24 hours after surgery

次要结局

  • Total analgesic pump drug use(From the end of surgery until removal of the analgesic pump,assessed up to 3 days)
  • Time of first use of remedial analgesics or analgesic pump(From the end of surgery until the date of first use of remedial analgesics or analgesic pumps,assessed up to 3 days)
  • Postoperative bilirubin level(Time 1 (Within 5 minutes of the surgery), Time 2 (1 day post-surgery), Time 3 (2 days post-surgery))
  • Postoperative creatinine level(Time 1 (Within 5 minutes of the surgery), Time 2 (1 day post-surgery), Time 3 (2 days post-surgery))
  • Postoperative liver enzyme level(Time 1 (Within 5 minutes of the surgery), Time 2 (1 day post-surgery), Time 3 (2 days post-surgery))
  • Postoperative cortisol level(Time 1 (Within 5 minutes of the surgery), Time 2 (1 day post-surgery), Time 3 (2 days post-surgery))
  • Postoperative IL-6 level(Time 1 (Within 5 minutes of the surgery), Time 2 (1 day post-surgery), Time 3 (2 days post-surgery))
  • Postoperative IL-8 level(Time 1 (Within 5 minutes of the surgery), Time 2 (1 day post-surgery), Time 3 (2 days post-surgery))

研究者

发起方
The Fourth Affiliated Hospital of Zhejiang University School of Medicine
申办方类型
Other
责任方
Sponsor

相似试验