Ciprofol Versus Propofol for the Prevention of Hypoxia During Gastrointestinal Endoscopy Procedures in Overweight Patients: A Multicenter, Randomized, Controlled Trial.
Summary
In overweight patients undergoing GI endoscopy, ciprofol sedation reduced the combined incidence of hypoxia and severe hypoxia compared with propofol. Secondary outcomes favored ciprofol, including less injection pain and fewer corrective measures for hypoxia, while endoscopy success was comparable.
Key Findings
- Ciprofol reduced the total incidence of hypoxia and severe hypoxia versus propofol in overweight patients during GI endoscopy.
- Secondary outcomes supported ciprofol with lower injection pain and fewer corrective hypoxia interventions.
- Endoscopy success rates were comparable between groups.
Clinical Implications
For overweight patients undergoing GI endoscopy, ciprofol may be preferred over propofol to lower hypoxia risk, with similar procedural success. Institutions should consider updating sedation protocols and monitoring workflows accordingly.
Why It Matters
This large multicenter RCT directly informs sedative selection in a high-volume procedural setting, demonstrating a clinically meaningful reduction in hypoxia with ciprofol.
Limitations
- Abstract does not report exact event rates or effect sizes in the public summary
- Conducted in a single country; generalizability to other populations requires caution
Future Directions
Head-to-head trials in diverse populations, mechanistic studies on respiratory physiology under ciprofol, and cost-effectiveness analyses to guide formulary adoption.
Study Information
- Study Type
- RCT
- Research Domain
- Treatment
- Evidence Level
- II - Individual multicenter randomized controlled trial
- Study Design
- OTHER