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Comparison of Ciprofol and Propofol on Recovery Quality After Sedation for Painless Colonoscopy: A Randomized Controlled Trial

Comparison of Ciprofol and Propofol on Recovery Quality After Sedation for Painless Colonoscopy: A Randomized Controlled Trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600117655
Enrollment
Unknown
Registered
2026-01-27
Start date
2026-01-31
Completion date
Unknown
Last updated
2026-02-02

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

Conditions

Colitis

Interventions

Propofol group:Intravenous injection of sufentanil 0.1 µg/kg + propofol 2 mg/kg for induction of sedation + subsequent additional doses of propofol 0.6 mg/kg, maintaining MOAA/S score <= 3.
Ciprofol group:Intravenous injection of sufentanil 0.1 µg/kg + ciprofol 0.5 mg/kg for induction of sedation + subsequent additional doses of ciprofol 0.15 mg/kg, maintaining MOAA/S score <= 3.

Sponsors

Jinjiang Municipal Hospital (Shanghai Sixth People's Hospital Fujian)
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Age 18-80 years 2. American Society of Anesthesiologists (ASA) physical status classification I-III 3. Scheduled for outpatient colonoscopy

Exclusion criteria

Exclusion criteria: 1. 1. The patient refuses to participate. 2. Unable to walk independently for any reason. 3. Body Mass Index (BMI) >30 kg/m^2. 4. Obstructive sleep apnea syndrome 5. Contraindications or allergies to research drugs 6. Colonoscopic treatment, such as: endoscopic polypectomy, endoscopic submucosal dissection, etc. 7. History of mental illness 8. History of neurological diseases 9. Drug abuse or chronic alcohol addiction 10. For any reason, one cannot participate in the research, such as: difficulty in language comprehension, cognitive impairment, etc

Design outcomes

Primary

MeasureTime frame
Time from the end of colonoscopy to meeting discharge criteria;

Secondary

MeasureTime frame
Induction time;Colonoscopy procedure time;Emergence time;Fatigue level after awakening;Endoscopist satisfaction;Anesthesiologist satisfaction;Patient satisfaction;

Countries

China

Contacts

Public ContactLin Yue

Jinjiang Municipal Hospital(Shanghai Sixth People's Hospital Fujian)

751524972@qq.com+86 152 0597 0421

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 7, 2026