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Efficacy and safety of ciprofol versus propofol in anesthesia for painless colonoscopy

Efficacy and safety of ciprofol versus propofol in anesthesia for painless colonoscopy

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200061814
Enrollment
Unknown
Registered
2022-07-03
Start date
2022-06-20
Completion date
Unknown
Last updated
2023-09-18

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

Conditions

colonoscopy patient

Interventions

Propofol Group:Propofol

Sponsors

The First Affiliated Hospital of University of Science and Technology of China
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Aged 18-65 years, no gender restrictions; 2. ASA I-III grade; 3. Subjects who are scheduled to undergo painless colonoscopy; 4. Sign informed consent.

Exclusion criteria

Exclusion criteria: 1. Those who are allergic to drugs; those who have contraindications to propofol; 2. Those who have chronic pain and long-term use of analgesics, psychiatric drugs (including opioids, NSAIDs, sedatives, antidepressants), and alcohol abusers; 3. BMI > 30 kg/m2; 4. Abnormal liver and kidney function before surgery; 5. Suffering from esophageal reflux disease; 6. Using sedative or analgesic drugs 24 hours before surgery; 7. Subjects with chronic lung disease; 8. Pregnant or parturient; 9. Suspicious difficulty Airway patients; 10. Participated in other drug trials within three months.

Design outcomes

Secondary

MeasureTime frame
Endoscopy physician satisfaction score;Injection pain;Respiratory depression;Anesthesia recovery time;Modified Aldrete score after awakening;

Primary

MeasureTime frame
Patient Satisfaction Score;

Countries

China

Contacts

Public ContactSheng Wang

The First Affiliated Hospital of University of Science and Technology of China

iamsheng2020@ustc.edu.cn+86 18935701573

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 6, 2026