colonic spasm
Conditions
Interventions
Contral group (Group C):transcutaneous electrical acupoint stimulation and comfort therapy
TEAS group (Group T):transcutaneous electrical acupoint stimulation
Sponsors
The First Affiliated Hospital of Zhengzhou University
Eligibility
Sex/Gender
All
Age
18 Years to 65 Years
Inclusion criteria
Inclusion criteria: 1. Patients scheduled for painless colonoscopy, aged 18-65 years; 2. American Society of Anesthesiologists (ASA) grade I-II; 3. No anticholinergic drugs, opioid analgesics or gastrointestinal motility regulators have been used in the past two weeks; 4. Written informed consent was obtained prior to participation in the study; 5. Body mass index (BMI) 18-30 kg/m^2.
Exclusion criteria
Exclusion criteria: 1. Special populations, such as pregnant women, patients with psychiatric disorders, or patients unable to cooperate with treatment; 2. Patients with severe respiratory, circulatory, or endocrine diseases, as well as those with abnormal liver or renal function; 3. Patients with preoperatively intractable abdominal pain or known intestinal motility disorders; 4. Patients with skin lesions or local infections, which render percutaneous electrical stimulation unfeasible; 5. Patients with allergy or intolerance to electrical stimulation therapy.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Incidence of colonic spasm; | — |
Secondary
| Measure | Time frame |
|---|---|
| Duration of colonic spasm;Postoperative pain intensity;Incidence of intraoperative adverse events;Ntraoperative polyp detection rate and number of detected polyps;Colonoscope insertion time;Patient awakening time;Postoperative adverse events;Patient satisfaction VAS scores;Endoscopist satisfaction VAS scores; | — |
Countries
China
Contacts
Public ContactNa Xing
The First Affiliated Hospital of Zhengzhou University
Outcome results
None listed