Acupuncture anesthesia under colonoscopy
Conditions
Interventions
sham acupuncture group:sham acupuncture
acupuncture group:acupuncture
Sponsors
Department of Anesthesiology General Hospital of Tianjin Medical University
Eligibility
Sex/Gender
All
Age
18 Years to 65 Years
Inclusion criteria
Inclusion criteria: Age = 18 and = 65 years old with no restriction on gender; Patients receiving painless colonoscopy diagnosis and treatment; ASA (American Society of Anesthesiologists) physical status classification of I or II; BMI (Body Mass Index) > 18 kg/m² and < 28 kg/m²
Exclusion criteria
Exclusion criteria: Patients planned for endotracheal intubation (including laryngeal mask); Patients requiring complex endoscopic diagnostic and therapeutic procedures; Patients with a history of intestinal stenosis or adhesion; Patients with acute heart failure; unstable angina pectoris; myocardial infarction within 6 months prior to screening; Patients with severe respiratory lesions; Patients with psychiatric disorders a history of long-term use of psychiatric medications and cognitive dysfunction; Patients judged to have difficult airway management (Modified Mallampati Score of Grade IV); Patients with severely impaired functions of vital organs such as the liver and kidneys; Patients with a history of drug abuse drug addiction or alcoholism within 2 years prior to the screening period where alcoholism is defined as an average daily consumption of more than 2 units of alcohol (1 unit = 360 mL of beer or 45 mL of spirits with 40% alcohol content or 150 mL of wine); Patients who have not received regular antihypertensive treatment or have poorly controlled blood pressure (sitting systolic blood pressure =160 mmHg or =90 mmHg and/or sitting diastolic blood pressure =100 mmHg during the screening period); Patients taking benzodiazepines and/or opioids daily for a month or intermittently within the past three months; Patients allergic to or having contraindications for opioids propofol and other related drug components; Pregnant or lactating women; Patients (including males) planning to conceive within 3 months; Patients who have participated as subjects in any clinical trial within the past 3 months; Patients deemed unsuitable for participation in this trial by the investigator
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The dosage of propofol per kilogram of body weight per minute; | — |
Secondary
| Measure | Time frame |
|---|---|
| Dosage of propofol per kilogram of body weight;Evaluation of sedation quality;The total dosage of propofol and the administration of additional doses;Evaluation of Colonoscopy Quality;Evaluation of anesthesia safety;Evaluation of patient and physician satisfaction; | — |
Countries
China
Contacts
Public ContactChunyan Wang
Department of Anesthesiology General Hospital of Tianjin Medical University
Outcome results
None listed