Actively Recruiting

Phase Not Applicable
Age: 18Years - 64Years
All Genders
ID07517484

Effects and Mechanisms of Ambient Light Intensity on the Depth of General Anesthesia

Led by Peking University People's Hospital · Updated on 2026-05-29

66

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

This clinical trial investigates how different light conditions affect sedation depth during general anesthesia. The study aims to understand whether light exposure changes the amount of anesthetic drugs needed and the mechanisms behind this effect. Participants are adults aged 18 to 65 years with certain health status and body mass index ranges. Participants are randomly assigned to one of two groups: the light-shielded group or the non-light-shielded group. Those in the light-shielded group wear an opaque eye mask starting 30 minutes before anesthesia and continue wearing it until sedative medications are stopped. The other group receives no intervention related to light exposure. Throughout the surgery, researchers will record induction drug doses, induction time, total anesthetic dosage during surgery, and emergence time from anesthesia. These measurements help assess how light exposure influences anesthesia. The study runs until June 2026, with follow-up and monitoring during the perioperative period.

CONDITIONS

Brief Title

Light and Anesthesia

Who Can Participate

Age: 18Years - 64Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age between 18 and 65 years, regardless of gender
  • ASA physical status I or II
  • Body mass index between 18.5 and 28
  • Signed written informed consent
Not Eligible

You will not qualify if you...

  • Blindness or history of photosensitivity disorders
  • Need for medication for sleep or history of sleep disorders
  • Presence of neurological diseases
  • Pregnancy
  • Severe liver or kidney dysfunction
  • History of anesthetic drug abuse or alcohol abuse
  • History of adverse anesthesia events such as difficult airway or allergy to anesthetic agents

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

Implementation

Duration - Perioperative period

Participants in the light-shielded group wear an opaque eye mask 30 minutes prior to induction of general anesthesia and continue to do so until the sedative medications are stopped.

1 perioperative visit (in-person)

Trial Site Locations

Total: 1 location

1

Peking University People's Hospital

Beijing, China, 100044

Actively Recruiting

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Research Team

Y

Yi Feng, Ph.D

X

Xiaoyan Li, Ph.D

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

OTHER

Number of Arms

2

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Published Research Related To This Trial

Circadian differences in emergence from volatile anaesthesia in mice: involvement of the locus coeruleus noradrenergic system.

Dan Wang, Yujie Huang, Xinxin Wang...

https://pubmed.ncbi.nlm.nih.gov/32807382

Association between light at night, melatonin secretion, sleep deprivation, and the internal clock: Health impacts and mechanisms of circadian disruption.

Yvan Touitou, Alain Reinberg, David Touitou

https://pubmed.ncbi.nlm.nih.gov/28214594

Exposure to Short Wavelength-Enriched White Light and Exercise Improves Alertness and Performance in Operational NASA Flight Controllers Working Overnight Shifts.

Laura K Barger, Jason P Sullivan, Steven W Lockley...

https://pubmed.ncbi.nlm.nih.gov/33065729