跳至主要内容
临床试验/CTIS2023-509503-33-00
CTIS2023-509503-33-00进行中(未招募)1 期

Randomized and controlled clinical trial of the efficacy and safety of the use of lidocaine and magnesium sulfate for lung resection surgery using Video-Assisted Thoracic Surgery (VATS)

Clinica Universidad De Navarra0 个研究点目标入组 128 人开始时间: 2024年1月30日最近更新:

试验速览

阶段
1 期
状态
进行中(未招募)
发起方
入组人数
128

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
18 至 65+(—)
性别
All

入选标准

  • Patients undergoing lung tumor resection surgery using video-assisted thoracoscopy., The patient must be 18 years of age or older., The patient, or his or her representative, has given consent to participate in the study., The patient must, in the opinion of the investigator, be able to comply with all the requirements of the clinical trial.

排除标准

  • Patients who have previously been diagnosed with chronic pain prior to surgery., Patients unable to clearly understand the objectives and methodology of the study., Patients with chronic kidney damage with glomerular filtration < 60 ml/min (stage III-V)., Patients with liver dysfunction with total bilirubin > 3mg/dL., Expected surgery lasting more than 6 hours or no extubation plan immediately after surgery., Patients with < 45kg and > 100kg., Pregnant or breastfeeding women., History of hypersensitivity to any of the components of lidocaine or magnesium sulfate., Patients who for some medical reason are contraindicated in the use of lidocaine or magnesium sulfate., Patients who are taking analgesics (paracetamol or non-steroidal anti-inflammatory drugs or opioids) in the 7 days prior to surgery., History of alcohol or drug abuse or psychiatric illness., History of Congestive Heart Failure or ejection fraction <50% or atrioventricular heart block., Disease of the central nervous system., Porphyria.

研究者

发起方
Clinica Universidad De Navarra

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