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Effect of three intravenous infusion rates of propofol for Sedation for outpatient upper gastrointestinal endoscopy

Effect of three intravenous infusion rates of propofol for Sedation for outpatient upper gastrointestinal endoscopy

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-TRC-14004786
Enrollment
Unknown
Registered
2014-06-04
Start date
2014-06-25
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

upper gastrointestinal endoscopy

Interventions

Three groups:different administate rate of propofol

Sponsors

Second Affiliated Hospital of Jiaxing College, Jiaxing
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: American Society of Anesthesiologists' physical status grade I–III; aged 19–60 years outpatient upper gastrointestinal endoscopy

Exclusion criteria

Exclusion criteria: To be had a history of sleep apnea, severe respiratory, cardiovascular, disease, with a previous history of alcohol or sedative overdose, or with a history of central nervous system abnormalities.

Design outcomes

Primary

MeasureTime frame
BIS;—

Countries

China

Contacts

Public ContactHongmei Zhou

Second Affiliated Hospital of Jiaxing College, Jiaxing

lvminglyk@163.com+86 15821234563

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Mar 13, 2026