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临床试验/CTRI/2022/09/045393
CTRI/2022/09/045393尚未招募4 期

“Effect of Addition of Buprenorphine or Dexamethasone or Dexmedetomidine to Levobupivacaine on Postoperative Analgesia in Ultrasound guided transversus abdominis plane block in patients undergoing unilateral Inguinal Hernia Repair: a Prospective Randomized Double Blind Controlled Trial

srilakshmi narayana institute of medical sciences1 个研究点 分布在 1 个国家目标入组 90 人开始时间: 2022年9月15日最近更新:

试验速览

阶段
4 期
状态
尚未招募
发起方
入组人数
90
试验地点
1
主要终点
The primary outcomes of the study were the time taken for the first analgesic dose

研究概览

简要总结

Effect of addition of buprenorphine or dexamethasoneor dexmedetomidine to levobupivacaine on postoperative analgesia in ultrasoundguided transversus abdominis plane block in patients undergoing unilateralinguinal hernia repair: a prospective randomized double blind controlled trial is the study.90 patients aged between 18to 70 years with the American Society of Anesthesiologists classification (ASA)class 1 and 2 candidates for elective surgery under regional anesthesia at SriLakshmi Narayana Institute Of Medical Sciences with Inclusioncriteria :Patients willing to participate in the  study,ASA I &II,Patient age 18-70 years of either sex and Elective  surgery under general anesthesia withendotracheal intubation cases

Exclusioncriteria : has ASA 3 or more,Patients with history of risk factorsfor perioperative aspiration of gastric contents,history of chronic obstructive pulmonarydisease, asthma,history of recent respiratoryinfections,duration of surgery more than 3 h wereexcluded from the study, Pregnant and lactating mother and with study variables include General parameters i.e. Age, Gender, weight, heightand  Duration of surgery and duration ofanesthesia.the time taken to request for the first analgesic,totalrescue analgesic doses in the first 24 h, and the NRS score(0 = no pain, 10 =intolerable pain) just after the TAP block and at intervals of e  at intervals of 0,2,4,6,8,10,12,15,18,21and 24hrs postoperatively.Statistical analysis were performed using theIBM Statistical Package for the Social Sciences (SPSS) for windows, version22.0 (SPSS Inc., USA). Numerical data were analyzed by using an unpairedStudents t-test. Categorical data were analyzed by the chi square test orFisher’s exact test as appropriate. The differences among the 3 groups wereanalyzed by using the one-way analysis of variance (ANOVA) test.

研究设计

研究类型
Interventional
分配方式
Computer generated randomization
盲法
Participant, Investigator and Outcome Assessor Blinded

入排标准

年龄范围
18.00 Year(s) 至 70.00 Year(s)(—)
性别
All

入选标准

  • Patients willing to participate in the study ASA I &II.
  • Elective surgery under general anesthesia with endotracheal intubation cases.

排除标准

  • ASA 3 or more Patients with history of risk factors for perioperative aspiration of gastric contents, history of chronic obstructive pulmonary disease, asthma, history of recent respiratory infections, duration of surgery more than 3 h were excluded from the study.
  • Pregnant and lactating mother.

结局指标

主要结局

The primary outcomes of the study were the time taken for the first analgesic dose

时间窗: 2, 4, 6, 8, 10 12, | 15, 18, 21, and 24 h. aftter tap block

次要结局

  • total rescue analgesic doses in the first 24 h, and the NRS score.(24 hrs postoperatively)

研究者

发起方
srilakshmi narayana institute of medical sciences
申办方类型
Private medical college

研究点 (1)

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