Reinforcement Learned Automatic Anesthesia System During Painless Gastrointestinal Endoscopy

Last updated: May 8, 2025
Sponsor: Boston Intelligent Medical Research Center, Shenzhen United Scheme Technology Co., Ltd.
Overall Status: Active - Recruiting

Phase

N/A

Condition

Anesthesia

Treatment

General Anesthesia (GA)

AI Controlled General Anesthesia

Clinical Study ID

NCT06857344
SZUS2025001
  • Ages 18-65
  • All Genders
  • Accepts Healthy Volunteers

Study Summary

The goal of this clinical trial is to compare the performance difference between trained model and clinical professionals in anesthesia control during gastrointestinal endoscopy. The participants would include adults aged between 18-65 years old with ASA scores I-II. The main questions it aims to answer are:

  • Can AI model successfully and safely perform anesthesia during gastrointestinal endoscopy?

  • Researchers hypothesis that anesthesia performed by professionals is not inferior to those performed by AI model.

The researchers will compare the results of the AI group with the traditional group to see if both groups have similar success rates in performing anesthesia.

Participants will fast for 8 hours before the procedure, and drinking water will be prohibited for 2 hours after taking the intestinal purgatives.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • American Society of Anesthesiologists (ASA) physical status class I-II

  • Expected operation duration less than 1 hour

Exclusion

Exclusion Criteria:

  • History of cardiac, hepatic, renal, or metabolic disorders (e.g., diabetes,hypertension, sleep apnea)

  • Known allergy to opioids or ciprofloxacin components

  • Cachexia

  • Hypothermia; history of narcotic abuse; chronic alcoholism; obesity (BMI >30);patients with apnea

  • Current pregnancy or lactation

  • History of substance abuse or alcohol dependence

  • Participation in any other drug clinical trial within the past 3 months

  • Obesity (BMI >30 kg/m²)

  • Procedure termination due to gastric retention or inadequate bowel preparation

Study Design

Total Participants: 164
Treatment Group(s): 2
Primary Treatment: General Anesthesia (GA)
Phase:
Study Start date:
May 01, 2025
Estimated Completion Date:
October 01, 2025

Connect with a study center

  • Anxi County Hospital

    Anxi, Fujian
    China

    Active - Recruiting

  • Jinjiang Hospital

    Jinjiang, Fujian
    China

    Active - Recruiting

  • Xinzheng Public People's Hospital

    Xinzheng, Henan
    China

    Active - Recruiting

  • Henan Provincial People's Hospital

    Zhengzhou, Henan
    China

    Active - Recruiting

  • Zhengzhou Central Hospital

    Zhengzhou, Henan
    China

    Active - Recruiting

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