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临床试验/NCT07244757
NCT07244757已完成不适用

Comparison of Two Dosing Regimens of Intravenous Ketorolac for Post-Cesarean Pain Control: A Randomized Controlled Trial

Cairo University1 个研究点 分布在 1 个国家目标入组 125 人开始时间: 2025年12月1日最近更新:
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
125
试验地点
1
主要终点
numeric rating scale at rest

研究概览

简要总结

we aim to compare the analgesic efficacy of two intravenous ketorolac dosing regimens as part of a multimodal analgesic protocol that includes local wound infiltration for postoperative pain management after elective cesarean delivery.

详细描述

Spinal anesthesia will be achieved by injecting 10 mg hyperbaric bupivacaine 0.5% plus 25 mcg fentanyl Prophylactic vasopressor will be administered in all patients, Following delivery, all patients will receive a single dose of dexamethasone (8 mg) along with the first dose of intravenous ketorolac. Subsequent ketorolac doses will be administered every 8 hours.

After closing the fascia, the subcutaneous layer will be infiltrated with 30 mL of 0.25% bupivacaine.

Postoperatively, if the Numeric rating scale is > 3, intravenous nalbuphine 0.1 mg/kg titrated to response, with maximum single dose of 20 mg and maximum daily dose of 160 mg.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 35 Years(Adult)
性别
Female
接受健康志愿者

入选标准

  • full-term, singleton, pregnant women,
  • aged 18-35 years,
  • scheduled for elective cesarean delivery under spinal anesthesia

排除标准

  • American Society of Anesthesiologists (ASA) physical class III or more
  • multiple gestation. Patients with a history of allergy to any of the study drugs,
  • renal impairment,
  • gastrointestinal bleeding or ulceration
  • inflammatory bowel disease,
  • chronic pain or regular opioid use.
  • Inability to comprehend the numeric pain scale (NRS) or the ObsQoR-11 score
  • requirement for conversion to general anesthesia after spinal anesthesia

研究组 & 干预措施

ketorolac 30

Active Comparator

patients will receive intravenous ketorolac at 30 mg/8 h postoperatively

干预措施: Ketorolac 30 mg (Drug)

ketorolac 15 mg

Active Comparator

patients will receive intravenous ketorolac at 15 mg/8 h postoperatively

干预措施: Ketorolac 15mg (Drug)

结局指标

主要结局

numeric rating scale at rest

时间窗: 6 hours postoperatively

the patient rates their pain on a scale of 0 to 10, with 0 being "no pain" and 10 being the "worst pain imaginable"

次要结局

  • numeric rating scale at rest(at 30 minutes, 12-, 18-, and 24 hours postoperatively)
  • total nalbuphine consumption(from 0.5 hour postoperatively to 24 hour postoperatively)
  • time to first analgesic requirement(time from immediately postoperatively to time of first analgesic requirement during the first 24 hours)
  • numeric rating scale during movement(at 30 minutes, 6-, 12-, 18-, and 24 hours postoperatively)
  • ObsQoR-11 score(24 hour postoperatively)
  • patient's satisfaction(24 hour postoperatively)

研究者

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

Ahmed Hasanin

professor

Cairo University

研究点 (1)

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