induction of anesthesia
Conditions
Interventions
Control group (P) group:Propofol 2mg/Kg
Fospropofol Disodium group (F1) group:Fospropofol Disodium 12.5mg/kg
Fospropofol Disodium group (F2) group:Fospropofol Disodium 15mg/kg
Fospropofol Disodium group (F3) group:Fospropofol Disodium 17.5mg/kg
Fospropofol Disodium group (F4) group:Fospropofol Disodium 20mg/kg
Sponsors
Neijiang First People's Hospital
Eligibility
Sex/Gender
All
Age
65 Years to 100 Years
Inclusion criteria
Inclusion criteria: 1. Age: >= 65 years old; 2. ASA classification: Grade I - III; 3. Patients requiring ERCP; 4. Voluntary participants in this study; 5. Patients with complete relevant examinations.
Exclusion criteria
Exclusion criteria: 1. Patients who are allergic to the relevant anesthetic drugs; 2. Patients with potentially difficult airways; 3. Patients with severe functional impairments of organs such as the heart, lungs, liver, and kidneys; 4. Patients who have long-term drug abuse; 5. Patients with any diseases that make them difficult to cooperate; 6. Other cases that are not suitable for participating in this study.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The success rate of sedation 5 minutes after the first anesthesia induction; | — |
Secondary
| Measure | Time frame |
|---|---|
| Anesthesia induction time;Endoscopic operation time;Anesthesia recovery time; | — |
Countries
China
Contacts
Public ContactXingcong Zhang
Neijiang First People's Hospital
Outcome results
None listed