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临床试验/CTRI/2025/11/097627
CTRI/2025/11/097627尚未招募不适用

Association between Perioperative Pupillary Parameters and Opioid Analgesic Requirements in Adult Spine Surgery A Prospective Observational Study

Ranjana Sure1 个研究点 分布在 1 个国家目标入组 100 人开始时间: 2025年12月8日最近更新:

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
100
试验地点
1

研究概览

简要总结

Pupil size reflects the balance between sympathetic and parasympathetic systems. Nociceptive stimulation increases sympathetic discharge which in turn dilates pupil and increases pupillary size that is inhibited by opioids in dose dependent fashion.The pupil diameter increases in response to pain regardless of gender and anxiety level. Clinically measured pupillary size is subjective and has interobserver variability . Hence hand held pupillometer is used. More the pupillary size more the analgesics required in intraoperative period to manage pain.

The aim of this study is to evaluate the association between perioperative pupillometry changes (delta pupillometry is equal to post-operative minus pre-operative pupillometry values) and the total dose of  intra-operative opioids and perioperative analgesics[ opioid and non opioid]

研究设计

研究类型
Observational

入排标准

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

入选标准

  • 1 ASA physical status I–III.
  • 2 Scheduled for elective spine surgery under general anaesthesia.
  • 3 Written informed consent obtained.

排除标准

  • 1 Pre-existing ocular pathology (example glaucoma, prior intraocular surgery, anisocoria).
  • 2 Neurological disease affecting pupillary function..
  • 3 Chronic opioid therapy (more than 3 months).
  • 4 Psychiatric illness interfering with pain reporting.
  • 5 Patients refusing participation.

研究者

发起方
Ranjana Sure
申办方类型
Other [Self sponsered]
责任方
Principal Investigator
主要研究者

Ranjana Sure

National Institute of Mental Health and Neurosciences

研究点 (1)

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