Skip to content

Safety and efficacy of ciprofol in painless gastrointestinal endoscopy

Observation on the application effect of ciprofol in painless gastrointestinal endoscopy

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400079864
Enrollment
Unknown
Registered
2024-01-15
Start date
2024-01-15
Completion date
Unknown
Last updated
2024-01-22

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

Conditions

Painless gastroenteroscopy

Interventions

Group C (cypofol group):After oxygen monitoring, 0.1µg/kg sufentanil was injected intravenously. One minute later, cyclopropofol 0.4mg/kg was slowly injected intravenously in group C, and the endoscop
group P (propofol group):After oxygen monitoring, 0.1µg/kg sufentanil was injected intravenously. One minute later, propofol 2mg/kg was administered slowly intravenously in group P. When BIS value was

Sponsors

Department of Anesthesiology, Honghui Hospital, Xi'an Jiaotong University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: (1) Patients who have undergone painless gastroscopy at our hospital on a scheduled basis; (2) Age range from 18 to 65 years old; (3) ASA level I-II; (4) 18kg/m2<BMI<30kg/m2; (5) The patient or their family members sign an informed consent form.

Exclusion criteria

Exclusion criteria: (1) Patients who are allergic to the investigational drug or have other contraindications; (2) Severe diseases of the heart, brain, lungs, liver, kidneys, lungs, and endocrine system.

Design outcomes

Primary

MeasureTime frame
Mean arterial pressure, heart rate, respiratory rate;

Secondary

MeasureTime frame
The success rate of first sedation and the addition rate of sedative drugs;

Countries

China

Contacts

Public ContactWang Fang

Department of Anesthesiology, Honghui Hospital, Xi'an Jiaotong University

2477557343@qq.com+86 139 9123 7605

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026