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临床试验/EUCTR2010-024402-35-GB
EUCTR2010-024402-35-GB进行中(未招募)1 期

Clinical effectiveness of Transversus Abdominis Plane (TAP) block as postoperative analgesic in patients undergoing laparoscopic colorectal surgery: a double blinded randomised controlled trial - Effective pain relief following laparoscopic colorectal surgery

Sussex NHS Research Consortium0 个研究点目标入组 80 人开始时间: 2012年4月2日最近更新:
适应症
相关药物

试验速览

阶段
1 期
状态
进行中(未招募)
发起方
入组人数
80

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
All

入选标准

  • Inclusion Criteria: All patients undergoing elective laparoscopic colorectal resectional procedures Patients undergoing colorectal procedure with or without stoma Patients of either sex Adult patients above 16 years of age Patients of any BMI Patients who have had neoadjuvant radiotherapy or chemoradiotherpay Patients of ASA I, ASA II and ASA III anaesthetic risk Patients who agree and sign the consent form to participate in this trial.
  • Are the trial subjects under 18? no
  • Number of subjects for this age range: 0
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range 40
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range 50

排除标准

  • Exclusion Criteria: Patients unable to give consent or refuse to participate in this study Patients under the age of 16 years Patients who are pregnant Patients undergoing an emergency operation Patients undergoing the procedure as a postoperative complication Procedures performed for complications or adverse events during the same hospital episode or performed in circumstances related to a primary and initial procedure. Patient is allergic to any medication used in local infiltration and/or morphine Patients with chronic pain syndrome Patients with severe hypotension such as cardiogenic or hypovolaemic shock Patients with severe hypertension.

研究者

发起方
Sussex NHS Research Consortium

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