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临床试验/NCT06513013
NCT06513013已完成2 期

Comparative Evaluation of Magnesium Sulphate Versus Neostigmine as an Adjuvant to Bupivacaine in Ultrasound Guided Transversus Abdominis Plane (TAP) Block as Postoperative Analgesia in Cesarean Section

Assiut University1 个研究点 分布在 1 个国家目标入组 68 人开始时间: 2023年12月20日最近更新:
适应症
干预措施

试验速览

阶段
2 期
状态
已完成
入组人数
68
试验地点
1
主要终点
comparasion of Postoperative NRS score for 24 hours between the two groups

研究概览

简要总结

The aim of this study is to compare the duration of analgesia obtained by addition of Neostigmine versus MgSO4 as adjuvants to bupivacaine in TAP block in patients undergoing Cesarean Section and to evaluate postoperative analgesic requirements, side effects and level of patient satisfaction.

详细描述

Caesarean section (CS) is one of the most operations in the world. Effective postoperative analgesia after it is very important because it encourages breast feeding and facilitates early ambulation and recovery. Postoperative analgesia is too important to prevent unwanted side effects such as venous thromboembolism, respiratory complications and increased hospital stay.Post Caesarean discomfort and pain is expected; so, the analgesic regimen should assure safe and efficient sedation. Commonly, opioids and NSAIDs are used for post caesarean pain relief. While dose dependent respiratory depression is the most discomforting side effect, other insignificant side effects such as gastrointestinal upset, pruritus and urinary retention can be annoying during the first hours of puerperium. The transversus abdominus plane (TAP) block has been used for postoperative pain relief in different abdominal surgeries as part of the multimodal anesthetic approach.It creates satisfactory somatic anesthesia with no visceral blockade. Its widespread use in abdominal surgeries is due to its technical simplicity and trustworthy analgesia .This block implies administering local anesthetic between the internal oblique muscle and transversus abdominis muscle, which is marked by the lumbar Petit triangle. The primary drawback of single-shot regional blocks is their short duration of action when administered with local anesthetic alone. Several adjuvants, including opioids, alpha 2 agonists,Neostigmine, N-methylD-aspartate (NMDA) receptor antagonists, and other drugs, have been utilized to extend the duration of blocks . Opioids are by far the most often used adjuvants, but they accompany a host of unpleasant side effects, such as respiratory depression, drowsiness, nausea, and vomiting. In some studies, using alpha 2 agonists such as Dexmedetomidine and Clonidine has been related to drowsiness and bradycardia .

MgSO4 is an N-methyl-D-aspartate (NMDA) receptor antagonist. It acts by non-competitive antagonism blocking the voltage-dependent ion channels.

The potential of neostigmine as an adjuvant in peripheral nerve block is through its action to increase acetylcholine at muscarinic junctions of peripheral nerves. 500 mcg neostigmine was used as adjuvant to local anesthetic in an axillary brachial plexus block leads to decreased pain and less use of analgesics in the first 24 hours postoperatively with no incidence of adverse effects

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
19 Years 至 40 Years(Adult)
性别
Female
接受健康志愿者

入选标准

  • Age from 19 to 40 years old
  • Singleton pregnencies with a gestational age of at least 37 weeks
  • American society of anesthesiologists (ASA) physical state I , II
  • patients undergoing spinal anesthesia for cesarean delivery via Pfannenstiel incision with exteriorization of the uterus.

排除标准

  • Patient's refusal
  • Age < 19 or > 40 years
  • Height<150 cm, weight < 60 kg, body mass index (BMI) ≥40 kg/m
  • Contraindications to spinal anesthesia (Coagulopathy, increased intracranial pressure, or local skin infection).
  • Cardio-respiratory conditions
  • Convulsions
  • Inability to comprehend or participate in the pain scoring system.
  • Bleeding diathesis
  • Known allergy to any drugs used in this study

研究组 & 干预措施

Group M "bupivacaine + normal saline + MgSO4"

Active Comparator

will receive 25 ml volume on each side ( 20 ml of 0.25% bupivacaine plus 5 ml of normal saline containing 250 mg of MgSO4 )

干预措施: transversus abdominis plane (TAP) block in cesarean section (Procedure)

Group M "bupivacaine + normal saline + MgSO4"

Active Comparator

will receive 25 ml volume on each side ( 20 ml of 0.25% bupivacaine plus 5 ml of normal saline containing 250 mg of MgSO4 )

干预措施: Magnesium sulfate (Drug)

Group D "bupivacaine + normal saline + Neostigmine"

Active Comparator

will receive 25 ml volume on each side ( 20 ml of 0.25% bupivacaine plus 5 ml of normal saline containing 500 mcg of Neostigmine

干预措施: transversus abdominis plane (TAP) block in cesarean section (Procedure)

Group D "bupivacaine + normal saline + Neostigmine"

Active Comparator

will receive 25 ml volume on each side ( 20 ml of 0.25% bupivacaine plus 5 ml of normal saline containing 500 mcg of Neostigmine

干预措施: Neostigmine (Drug)

结局指标

主要结局

comparasion of Postoperative NRS score for 24 hours between the two groups

时间窗: 24 hours postoperative

NRS Score: used to assess pain intensity (13). It is one of the most commonly used pain scales in medicine. The NRS consists of a numeric version of the visual analog scale. It is a horizontal line with an eleven point numeric range. It is labeled from zero to ten, with zero being an example of someone with no pain and ten being the worst pain possible (Figure 2). This scale can be administered verbally. Rescue analgesia will be nalbuphine 0.1 mg/kg IV when the NRS ≥ 4.

次要结局

  • postoperative hemodynamic parameters(24 hours postoperative)
  • time required for the first rescue analgesia(24 hours postoperative)
  • total amount of rescue analgesic consumption duringfirst 24 hours postoperatively(24 hours postoperative)
  • patient satisfacation score(24 hours postoperative)
  • PONV intensity by postoperatively:(24 hours postoperative)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Alfarouk Ayman Farouk Omar

resident

Assiut University

研究点 (1)

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