Participation in Painless Gastrointestinal Endoscopy
Conditions
Interventions
Sufentanil Group:Sufentanil + Propofol
Buccal Acupuncture Treatment Group:Buccal Acupuncture + Propofol
Control Group:Propofol
Sponsors
Yuying Children's Hospital, the Second Affiliated Hospital of Wenzhou Medical University
Eligibility
Sex/Gender
All
Age
18 Years to 65 Years
Inclusion criteria
Inclusion criteria: 1: Voluntarily participate in this clinical trial and sign the informed consent form. 2: American Society of Anesthesiologists (ASA) Physical Status Classification Grade I - II; 3: Patients scheduled for painless gastroenteroscopy are selected, regardless of gender.
Exclusion criteria
Exclusion criteria: 1: Age 65 years old 2: Obesity (BMI > 30) 3: With severe hepatic or renal dysfunction, or diabetes mellitus. 4: Patients who have been taking analgesic drugs for a long time or are currently taking non-steroidal anti-inflammatory drugs recently. 5: With a history of drug allergy or metal allergy. 6: Abnormal blood coagulation function 7: Facial skin infection 8: History of fainting during acupuncture 9: Severe cardiovascular and cerebrovascular diseases 10: The time of painless gastroenteroscopy exceeds 30 minutes.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The incidence of intraoperative body movement;Age of the subjects; | — |
Secondary
| Measure | Time frame |
|---|---|
| The incidence of oxygen desaturation;The duration of painless gastroenteroscopy;Preoperative heart rate;Mean arterial pressure at 3 minutes after anesthesia induction;Heart rate after awakening;The natural awakening time of the subjects;The incidence of mean arterial pressure less than 30% of the preoperative value after induction;ostoperative pain (Numeric Rating Scale, NRS) score;The incidence of dizziness during the PACU period;Preoperative mean arterial pressure (MAP);The incidence of nausea and vomiting during the PACU period.;Mean arterial pressure after awakening;The incidence of heart rate less than 30% of the preoperative value after induction;Total dosage of propofol;Gender of the subjects;Heart rate at 3 minutes after anesthesia induction; | — |
Countries
China
Contacts
Public ContactChaoqun Huang
Yuying Children's Hospital, the Second Affiliated Hospital of Wenzhou Medical University
Outcome results
None listed