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临床试验/NCT07141589
NCT07141589招募中不适用

Fentanyl Versus Ketorolac as an Adjuvant to Peribulbar Block for Anterior Segment Surgeries, A Prospective Double-blinded Randomized Controlled Study

Cairo University1 个研究点 分布在 1 个国家目标入组 168 人开始时间: 2024年8月25日最近更新:
干预措施
相关药物

试验速览

阶段
不适用
状态
招募中
入组人数
168
试验地点
1
主要终点
Duration of globe akinesia

研究概览

简要总结

This study aims to compare the efficacy of ketorolac and fentanyl as adjuvants to local anesthetics for anterior segment surgeries of the eye.

详细描述

Regional anesthesia for eye surgery includes peribulbar, retrobulbar, and sub-Tenon's blocks. Peribulbar block is commonly used due to a lesser incidence of serious complications such as globe perforation and retrobulbar hemorrhage.

Fentanyl is a synthetic opioid widely used as an adjuvant to local anesthetics to prolong its action and provide better postoperative analgesia. fentanyl fastens lid and globe akinesia and provides a better akinesia score.

Ketorolac is a non-steroidal anti-inflammatory drug (NSAID) that reduces the release of inflammatory mediators such as prostaglandins, thereby reducing afferent sensitivities and finally reducing pain. It is devoid of narcotic analgesic adverse effects such as sedation, nausea, and respiratory depression.

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
Double (Participant, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Age over 18 years old.
  • Both sexes.
  • American Society of Anesthesiologists (ASA) physical status I-III.
  • Scheduled to undergo operations for anterior segment surgeries of the eye under local (peribulbar) anesthesia.

排除标准

  • Patient's refusal.
  • Known allergy or hypersensitivity to aspirin or nonsteroidal anti-inflammatory medications.
  • Patients with contraindications to local anesthetics, such as high axial length or patients with high preoperative intraocular pressure.
  • If cases develop severe pain intraoperatively from the start, necessitating rescue analgesia and sedation or requiring conversion to general anesthesia.
  • Infection at the site of injection.
  • Patients with coagulopathies or on anticoagulants.
  • Impaired renal function.

研究组 & 干预措施

Fentanyl group

Experimental

Patients will receive a mixture of 3 ml lidocaine 2%, 3 ml bupivacaine 0.5%, and hyaluronidase 60 IU and fentanyl 20 μg diluted in normal saline to a total volume of 8 ml.

干预措施: Fentanyl + Lidocaine + Bupivacaine + Hyaluronidase (Drug)

Ketorolac group

Experimental

Patients will receive a mixture of 3 ml lidocaine 2%, 3 ml bupivacaine 0.5%, hyaluronidase 60 IU, and ketorolac 15 mg diluted in normal saline to a total volume of 8 ml.

干预措施: Ketorolac + Lidocaine + Bupivacaine + Hyaluronidase (Drug)

Control group

Active Comparator

Patients will receive a mixture of 3 ml lidocaine 2%, 3 ml bupivacaine 0.5%, hyaluronidase 60 IU diluted in normal saline to a total volume of 8 ml.

干预措施: Lidocaine + Bupivacaine + Hyaluronidase (Drug)

结局指标

主要结局

Duration of globe akinesia

时间窗: 10 minutes after injection

Assessment of Globe akinesia will be assessed at 2, 5 and 10 minutes after injection with a 12-point scale. Each of the four rectus muscles and each lid score from 0 to 2; 0 = total akinesia, 1 = partial akinesia, 2 = no akinesia)

次要结局

  • Time of first rescue analgesia(6 hours postoperatively)
  • Heart rate(Intraoperatively)
  • Blood pressure(Intraoperatively)
  • Onset of globe akinesia(10 minutes after injection)
  • Onset of corneal anesthesia(1 minute after injection)
  • Degree of pain(6 hours postoperatively)

研究者

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

Aya Mohamed Abo Zied

Assistant Lecturer of Anesthesia, Surgical ICU and Pain Medicine, Faculty of Medicine, Cairo University, Cairo, Egypt.

Cairo University

研究点 (1)

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