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Studying how changes in the eyes pupil during spine surgery relate to the amount of pain medicine adults need

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

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2025/11/097627
Enrollment
100
Registered
2025-11-18
Start date
Unknown
Completion date
Unknown
Last updated
2025-12-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: M498- Spondylopathy in diseases classified elsewhere

Interventions

Intervention1: Nil: Nil

Sponsors

Ranjana Sure
Lead Sponsor

Eligibility

Inclusion criteria

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

Exclusion criteria

Exclusion criteria: 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.

Design outcomes

Primary

MeasureTime frame
To evaluate the association between perioperative pupillometry changes (delta pupillometry is equal to post-operative minus pre-operative pupillometry values) and the total intra-operative opioid dose titrated using Analgesia Nociception Index (ANI) in patients undergoing spine surgery.Timepoint: 24 hours

Secondary

MeasureTime frame
2. To evaluate whether baseline (pre-operative) pupillometry values are predictive of intra operative opioid requirements.Timepoint: 24 hours

Countries

India

Contacts

Public ContactRanjana Sure

National Institute of Mental Health and Neurosciences

drshwethanaik85@gmail.com9845118260

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026