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Observational analysis of the application effect and complications of cyclopofol and propofol in painless gastroscopy and colonoscopy operations

Observational analysis of the application effect and complications of cyclopofol and propofol in painless gastroscopy and colonoscopy operations

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600123904
Enrollment
Unknown
Registered
2026-04-30
Start date
2026-05-01
Completion date
Unknown
Last updated
2026-05-04

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

Conditions

Painless gastroscopy and colonoscopy

Interventions

Circopamine Group:None
Propofol Group:None

Sponsors

Wuhan University of Science and Technology Affiliated China Resources Wuhan Iron and Steel General Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1. ASA classification I-II 2. aged 18 to 60 years 3. BMI: 18-30 kg/m^2

Exclusion criteria

Exclusion criteria: 1. Patients with severe hypertension, cardiovascular and cerebrovascular diseases; 2. individuals with a history of opioid abuse, alcoholism, or mental illness; 3. those who have received sedative treatment within the past month.

Design outcomes

Primary

MeasureTime frame
Success rate of anesthesia induction;Vital signs (SBP, DBP, HR, SpO2);Injection pain;Time-related indicators (induction time, procedure time, awakening time, discharge time);Intraoperative awareness, nightmares, comfort level;—

Countries

China

Contacts

Public ContactWan Qing

Wuhan University of Science and Technology Affiliated China Resources Wuhan Iron and Steel General Hospital

289320836@qq.com+86 134 6996 3622

Outcome results

None listed

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