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NCT07749781Possibly a fitRecruiting

Smart monitoring software for safer sedation during endoscopy

Procedural SedationGastrointestinal Endoscopy

Part of Digestive system clinical trials.

This study tests a computer program that helps doctors watch your vital signs while you are sedated for a routine gastrointestinal procedure, with the goal of making sedation safer and more personalized.

Summary written for real people, not researchers, by Clin2.

Phase
N/A
Enrollment
120 people
Ages
18 years and older
Study type
Observational

Who can take part

  • You are 18 years or older.
  • Your physical health is classified as ASA I, II, or III (generally healthy or with mild to moderate illness).
  • You are scheduled for a non-emergency gastrointestinal endoscopy (such as a colonoscopy or upper endoscopy).
  • You will receive sedation through an IV line in your arm using two medications called propofol and remifentanil, given by a target-controlled infusion pump.
  • You do not have severe heart, lung, or nervous system disease that would interfere with monitoring, and you do not have a known difficult airway.
  • You can understand the study information and give written consent.

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

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