painless gastrointestinal endoscopy
Conditions
Interventions
Control group:Patients in sham group were treated by transcutaneous electrical acupuncture point stimulation at the Zu?sanli?(ST36) acupoint without an electrical current
TEAS group:Patients in TEAS group were treated by transcutaneous electrical acupuncture point stimulation at the Zu?sanli?(ST36) acupoint with an electrical current
Sponsors
Shanghai East Hospital
Eligibility
Sex/Gender
All
Age
65 Years to No maximum
Inclusion criteria
Inclusion criteria: 1. Aged >=65 years; 2. Patients undergoing painless gastrointestinal endoscopy; 3. American Society of Anesthesiologists (ASA) classification I or II.
Exclusion criteria
Exclusion criteria: 1. severe cardiac, pulmonary, hepatic, or renal insufficiency; 2. patients with chronic obstructive pulmonary disease; 3. pregnant and lactating patients; 4. abnormal blood clotting conditions; 5. allergic to drugs used in this study; 6. hypotensive patients (systolic blood pressure = 90 mmHg); 7. hypertensive patients (systolic blood pressure = 160 mmHg or diastolic blood pressure = 100 mmHg); 8. bradycardic patients ( Heart rate =50 beats/min); 9. Patients who refused to sign the informed consent; 10. Patients with hypoxemia (SpO2 <90%); 11. Patients with atrioventricular block; 12. Patients with psychosomatic diseases.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| incidence of hypoxia; | — |
Secondary
| Measure | Time frame |
|---|---|
| blood pressure;the degree of postoperative fatigue;heart rate;the depth of sedation;the number of postoperative vomiting;induction time of anesthesia;duration of painless gastrointestinal endoscopy;resuscitation time of anesthesia;the degree of postoperative pain;Physician Satisfaction;breathing;the number of postoperative nausea;Oxygen saturation;Patient satisfaction;propofol consumption; | — |
Countries
China
Contacts
Public ContactYang Hao
Outcome results
None listed