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临床试验/EUCTR2010-023350-37-GB
EUCTR2010-023350-37-GB进行中(未招募)不适用

Does intravenous lidocaine reduce opioid requirements after day case gynaecological laparoscopy? - Lidocaine for gynaecological laparoscopy v1.2

South Warwickshire NHS Foundation Trust0 个研究点目标入组 60 人开始时间: 2011年4月27日最近更新:
相关药物

试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
60

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional clinical trial of medicinal product

入排标准

性别
Female

入选标准

  • Adult female patients of ASA I or II scheduled for elective day case gynaecological laparoscopic procedure (laparoscopy +/- diathermy)with the exception of laparoscopic tubal ligation.
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range

排除标准

  • Inability to give informed consent Patients undergoing laparoscopy with tubal ligation Pregnancy Intolerance or allergy to non-steroidal anti inflammatory agents (NSAIDS) Intolerance or allergy to paracetamol Intolerance or allergy to lignocaine or other amide local anaesthetic agent Renal or hepatic impairment Congestive cardiac failure, sino-atrial disorders, atrio-ventricular block (all grades) Patients recieving treatment with beta blocking agents Patients receiving antipsychotic agents which prolong the QT interval Patients receiving treatment with Atazanavir, Lopinavir, Darunavir, Fosamprenavir Patients suffering from hypokalaemia (K+ < 3.5mmol/L) Acute porphyria Myasthenia gravis ASA status III or IV Patients prescribed pre-operative opioid analgesic agents Active gastro-oesphageal reflux disease, patients receiving regular cimetidine Patients scheduled for laparoscopy plus microwave endometrial ablation therapy

研究者

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