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Comparison of Anesthetic Safety of Propofol, Ciprofol, and Remimazolam in Painless Gastrointestinal Endoscopy Among Tumor Patients with Different BMI Stratifications

Comparison of Anesthetic Safety of Propofol, Ciprofol, and Remimazolam in Painless Gastrointestinal Endoscopy Among Tumor Patients with Different BMI Stratifications

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600125893
Enrollment
Unknown
Registered
2026-06-01
Start date
2026-06-01
Completion date
Unknown
Last updated
2026-06-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Tumor

Interventions

Propofol group (P group):Propofol 1.5 mg/kg IV bolus (slow injection in low BMI, lean body weight in obese) + Alfentanil 5 µg/kg
Ciprofol group (C group):Ciprofol 0.4 mg/kg IV bolus + Alfentanil 5 µg/kg
Remimazolam group (R group):Remimazolam 0.3 mg/kg IV bolus + Alfentanil 5 µg/kg

Sponsors

Yunnan Provincial Cancer Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Age 18-75 years. 2. ASA I-III. 3. BMI groups: (1) Low BMI group: 16.5 <= BMI < 18.5 kg/m^2 (2) Normal BMI group: 18.5 <= BMI < 24.0 kg/m^2 (3) Overweight and obese group: 24.0 kg/m^2 <= BMI < 40 kg/m^2 4. Sign informed consent form.

Exclusion criteria

Exclusion criteria: 1. Allergy to propofol, fospropofol, or benzodiazepines. 2. Severe cardiopulmonary dysfunction, severe liver or kidney dysfunction. 3. Communication disorders. 4. Presence of difficult airway risk (Mallampati classification grade IV). 5. Long-term use of sedatives or analgesics. 6. Morbid obesity (BMI > 40 kg/m^2).

Design outcomes

Primary

MeasureTime frame
Cyclic fluctuations;Respiratory depression;

Secondary

MeasureTime frame
Anesthetic efficacy;Adverse reactions;Awakening quality;

Countries

China

Contacts

Public ContactLi Shanshan

Yunnan Provincial Cancer Hospital

fengliya@163.com+86 135 7708 5164

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Jun 11, 2026