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临床试验/NCT06670508
NCT06670508
已完成
不适用

Efficacy of Erector Spinae Plane Block Versus Subcostal Transversus Abdominis Plane Block in Laparoscopic Nephrectomy: A Randomized Clinical Trial

Cairo University1 个研究点 分布在 1 个国家目标入组 70 人2023年10月1日

概览

阶段
不适用
干预措施
Subcostal Transversus Abdominis Plane block
疾病 / 适应症
Post Operative Pain Management
发起方
Cairo University
入组人数
70
试验地点
1
主要终点
The amount of morphine consumed within 6 hours postoperatively
状态
已完成
最后更新
昨天

概览

简要总结

The investigators hypothesize that erector spinae plane block is better than subcostal transversus abdominis plane block regarding postoperative pain management.

详细描述

Aim of the work: The purpose of this study is to compare erector spinae plane block to subcostal transversus abdominis plane block in laparoscopic nephrectomy regarding analgesic efficacy and postoperative morphine consumption. Statistical Analysis I. Sample size: Sample size was calculated using G-power software. A previous study (Hosgood et al., Transplantation 2012; 94: 520-525) reported that the amount of morphine used in the first 6 hours in patients received TAP block in nephrectomy was 12.4 ± 8.4. Assuming that the amount will change by 50% at least with the other block, a power of 80% and an alpha error of 0.05, the minimum sample size required will be 60 patients (30 in each group). We will increase it to 35 in each group to compensate for drop-outs. II. Statistical analysis: All measurement indexes will be expressed as mean ± SD/standard error of the mean or number (%). After analysis of normality of data distribution, normally distributed data will be compared by the independent sample t-test. Unpaired quantitative variables will be evaluated by the Student t-test and analysis of variance. The Mann-Whitney U test will be employed for intergroup comparison, and the Wilcoxon signed-rank test for comparison between different time points within the same group. Intergroup comparison of categorical variables will be performed by the chi-square test. Values of A P value less than 0.05 will be considered statistically significant. All data will be statistically analyzed by statisticians using the SPSS v28 software package (IBM Corp., Armonk, NY, USA).

注册库
clinicaltrials.gov
开始日期
2023年10月1日
结束日期
2024年5月15日
最后更新
昨天
研究类型
Interventional
研究设计
Parallel
性别
All

研究者

责任方
Principal Investigator
主要研究者

Mohamed Youssef

Assistant Professor

Cairo University

入排标准

入选标准

  • Patient age (\>18 and \<60)
  • Both sexes
  • American Society of Anesthesiologists (ASA) physical status classes I and II
  • Patients scheduled for total (radical) laparoscopic nephrectomy surgery

排除标准

  • Refusal of regional block
  • Patients with uncontrolled diabetes or hypertension
  • Patients with neurological, psychological disorders or those lacking cooperation
  • Patients with anatomic abnormalities at site of injection, skin lesions or wounds at site of proposed needle insertion.
  • Patients with bleeding disorders defined as (INR \>2) and/ or (platelet count \<100,000/µL)
  • Patients with hepatic disease e.g. liver cell failure or hepatic malignancy or hepatic enlargement.
  • Patients who are allergic to amide local anesthetics.
  • Cases converted to open surgery will also be excluded from the study

研究组 & 干预措施

Subcostal TAP Block

Group A, The patient was in the supine position then; the Subcostal TAP block was given by a high frequency linear ultrasound transducer (Siemens acuson x300 3-5MHz ultrasound). After skin preparation and isolation, the transducer was placed 2 cm sub-xiphoid, then moved along the subcostal edge to identify the rectus abdominis muscle and the transversus abdominis then, a blunted tip, 20-gauge, short bevel needle (Pajunk Sonoplex, Geisingen, Germany) was introduced in-plane 2-3 cm lateral to the transducer, under direct ultrasound visualization. After confirming the correct placement of the needle and the negative aspiration probe, the rest of the anaesthetic substance was injected along the subcostal line in the transversus abdominis plane 20 ml 0.25% bupivacaine on each side after aspiration to avoid intravascular placement, and the dissection of the plane was observed. The block was performed bilaterally.

干预措施: Subcostal Transversus Abdominis Plane block

ESP Block

Group B, the patient was placed in the prone position. Then, the Erector Spinae block was given by same ultrasound transducer . It was sagittaly placed against the target vertebral level (T7 transverse process) in the prone position and moved in approximately 3-cm lateral to the spinous process.. The Erector Spinae muscle and transverse process was identified, and a same blunted tip , 20-gauge, short bevel needle was advanced, using the in-plane approach, in cephalad-to-caudal direction, through the interfascial plane between the Erector Spinae and the underlying transverse process under strict aseptic precautions until the tip is deep to erector spinae muscle, as evidenced by visible hydro-dissection below the muscle plane. The block was performed bilaterally by injecting 40 mL of 0.25% bupivacaine (20 mL into each side) into the fascial plane between the deep surface of the Erector Spinae muscle and the transverse processes of the thoracic vertebrae laterally (specifically at T7).

干预措施: Erector Spinae Plane block

结局指标

主要结局

The amount of morphine consumed within 6 hours postoperatively

时间窗: Immediatly post operative for 6 hours

The amount of morphine consumed within 6 hours postoperatively

Cumulative morphine consumption at 6 hours postoperatively (co-primary endpoint)

时间窗: From end of surgery to 6 hours postoperatively

Total cumulative morphine consumption (in milligrams) measured at 6 hours postoperatively. Co-primary endpoint with 24-hour cumulative morphine consumption.

Cumulative morphine consumption at 24 hours postoperatively (co-primary endpoint)

时间窗: From end of surgery to 24 hours postoperatively

Total cumulative morphine consumption (in milligrams) measured at 24 hours postoperatively. Co-primary endpoint with 6-hour cumulative morphine consumption.

次要结局

  • p/f ratio postoperatively in both groups(after first 12, 24 hours postoperatively)
  • Failure rate in both groups(in first hour postoperatively)
  • Time taken to perform a successful block(30 minutes from time just after local anesthetic injection to successful site of incisions and dermatomal coverage)
  • Postoperative nausea and vomiting(Immediatly post operative for 24 hours)
  • Time to ambulate in both groups(Immediate 24 hours post-operative)
  • Incidence of postoperative pulmonary complication(chest x-ray Immediate 24 hours post-operative)
  • Incidence of complications (hematoma at the site of injection and local anesthetic toxicity) related to each block(Immediate 24 hours post-operative)
  • Time for first rescue analgesia in each block(Immediate 24 hours post-operative)
  • Total opioid consumption in each block(Immediate 24 hours post-operative)
  • Postoperative nausea and vomiting(Immediately post operative for 24 hours)

研究点 (1)

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