AI-controlled anesthesia during gastrointestinal endoscopy

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This clinical trial aims to compare the effectiveness of an AI-controlled anesthesia system against traditional anesthesia administered by clinical professionals during gastrointestinal endoscopy. Participants aged 18-65 with ASA scores I-II will be included, and the study will assess whether the AI model can safely and effectively manage anesthesia. The trial will involve fasting protocols and will evaluate success rates between the two groups to determine if AI can match or exceed the performance of human anesthetists.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* American Society of Anesthesiologists (ASA) physical status class I-II
* Expected operation duration less than 1 hour

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

Where it's running

• Anxi County Hospital
  Anxi, Fujian, China Recruiting
• Jinjiang Municipal Hospital, Shanghai Sixth People's Hospital Fujian Campus
  Jinjiang, Fujian, China Recruiting
• Xinzheng Public People's Hospital
  Xinzheng, Henan, China Recruiting
• Henan Provincial People's Hospital
  Zhengzhou, Henan, China Recruiting
• Zhengzhou Central Hospital
  Zhengzhou, Henan, China Recruiting

Study contacts

• Study coordinator: Dr. Chu
• Email: jimmynetchu@163.com
• Phone: +86 138 3810 0696

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

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  This study is testing if using ultrasound to check blood volume before surgery can help prevent low blood pressure right after anesthesia in patients who are at higher risk for complications.

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• Using different methods to help children feel less anxious during anesthesia induction

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.