跳至主要内容
临床试验/CTRI/2025/07/090851
CTRI/2025/07/090851尚未招募4 期

Comparison of ultrasound guided External Oblique Intercostal plane block and Transversus Abdominis plane block for postoperative analgesia in patients undergoing upper abdominal surgery under general anaesthesia

未提供1 个研究点 分布在 1 个国家目标入组 80 人开始时间: 2025年8月1日最近更新:

试验速览

阶段
4 期
状态
尚未招募
入组人数
80
试验地点
1
主要终点
Total 24 hour injection tramadol consumption

研究概览

简要总结

After preanaesthetic evaluation and obtaining written informed consent, patients will

be randomised by computer generated numbers into two groups.

Group E: Patients receiving External Oblique Intercostal Plane Block.

Group T: Patients receiving Transversus Abdominis Plane Block.

Patients in each group will receive 20 mL 0.125% bupivacaine with additive inj Fentanyl

2mcg/kg postoperatively. The patient will be shifted to operation theatre. Standard monitors

will be attached (noninvasive B.P, ECG, pulse oximetry, temperature probe) to record the

baseline vitals which will be monitored all through the procedure.

After obtaining wide bore intravenous access. Following injection Midaz 1.0 mg i/v,

injection Fentanyl 2.0 mcg/kg i.v., and injection propofol 2.0 mg/kg; check ventilation will be

done, and muscle relaxation will be attained using injection Vecuronium 0.1 mg/kg followed

by tracheal intubation with appropriate size endotracheal tube and put on mechanical

ventilation. Anaesthesia will be maintained with air, oxygen and sevoflurane with a MAC of

1-1.2

Vital signs ; HR, SBP, DBP, MAP, SpO2 will be recorded.

Injection fentanyl 1.0 mcg/kg will be administered if HR or MAP rise more than 20% of

baseline

Patients will receive injection paracetamol 15mg/kg after induction of anesthesia and 6

hourly till 24 hours after surgery

At the end of surgery respective ultrasound guided block will be given by an experienced

anaesthesiologist according to the study group allotted.

Injection ondansetron 0.1 mg/kg will be administered, and patient will be reversed

with injection neostigmine (0.05mg/kg) and injection glycopyrollate (0.01mg/kg).

Postoperatively HR, SBP, DBP, MAP and SpO2 heart rate, systolic blood pressure, diastolic

blood pressure, mean arterial pressure, SpO2, and NRS score (on scale of 1-10) will be

recorded at 5 min, 30 min, 60 min, 6hr, 12hr and 24 hr postoperatively by the anaesthesiologist

blinded to the group allotted.

Patients will be administered injection tramadol 50mg if NRS score is more than or equal to 4

研究设计

研究类型
Interventional
分配方式
Na
盲法
None

入排标准

年龄范围
18.00 Year(s) 至 65.00 Year(s)(—)
性别
All

入选标准

  • ASA grade 1 and 2 .
  • Elective upper abdominal surgeries .

排除标准

  • Known allergy to local anaesthetics.
  • Infection at injection site.
  • Patients undergoing chronic analgesia therapy.
  • Laparoscopic surgeries.
  • Patients with BMI more than 30.

结局指标

主要结局

Total 24 hour injection tramadol consumption

时间窗: 5 minutes, 30 minutes, 1 hour, 6 hours, 12 hours, and 24 hours after intervention.

次要结局

  • Time to first rescue analgesia postoperatively.(Patient satisfaction based on Likert scale (0-5).)

研究者

发起方
未提供
责任方
Principal Investigator
主要研究者

Naoshad Baqir

ABVIMS and Dr. Ram Manohar Lohia Hospital, New Delhi

研究点 (1)

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