Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-25 @ 3:52 AM
Ignite Modification Date:
2025-12-25 @ 3:52 AM
NCT ID:
NCT07081802
Eligibility Criteria:
Inclusion Criteria:
* Patients aged \>18 years with no severe preoperative gastrointestinal dysfunction (e.g., no chronic gastrointestinal diseases such as long-term constipation or diarrhea).
* Scheduled abdominal Grade IV surgeries (limited to liver, gallbladder, pancreas, stomach, or intestinal procedures) performed via open or laparoscopic approach.
* Preoperative American Society of Anesthesiologists (ASA) Physical Status Classification of I-III.
* Patients and their families fully understand the study's purpose, methods, potential risks/benefits, and provide signed informed consent.
Exclusion Criteria:
* Comorbid severe systemic diseases.
* Local skin abnormalities at acupoints (e.g.,broken skin, infection, allergies, or scarring).
* Preoperative long-term use (\>1 month) of gastrointestinal motility-affecting drugs (e.g., mosapride, domperidone) that cannot be discontinued, or allergies to TCM components/electrode materials.
* Psychiatric disorders or cognitive impairment rendering patients unable to comply with the study.
Elimination Criteria:
* Non-compliance with treatment protocols (e.g., receiving \<80% of planned sessions).
* Significant missing data.
* Occurrence of severe adverse events unrelated to the study intervention.
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Maximum Age:
80 Years
Study:
NCT07081802
Study Brief:
Protocol Section:
NCT07081802