CNClinicalTrials.govClinical trialNot applicableRecruiting
Transcutaneous Electrical Acustimulation on Postoperative Bowel Function Recovery in Elderly Patients
Official record
- Identifier
NCT07574502- Recruiting locations
country
China- Interventions studied
- TEAsham-TEA
- Lead sponsor
- Sir Run Run Shaw Hospital
- Target enrolment
- 190 participants
- Study type
- INTERVENTIONAL
- Phase
- Not applicable
- Status
- Recruiting
- First posted
- May 8, 2026
- Last updated on the registry
- Aug 14, 2026
- Age
- 65 Years
- Sex
- ALL
- Study contact
- The official record lists a study contact. Contact details are published there and are intentionally not copied to this page.
- Eligibility criteria
Reproduced verbatim from the official record. Eligibility is decided by the study team, never by this page.
Inclusion Criteria: * Age ≥ 65 years old. * Elective minimally invasive (laparoscopic or robotic) resection of colorectal cancer. * American Society of Anesthesiologists classification (ASA) 1-4. * Able to understand the research process and the use of various assessment scales, and able to communicate effectively with the researchers. * The patient voluntarily participates in this study and signs the informed consent form. Exclusion Criteria: * Previous history of abdominal gastrointestinal surgery. * Planned for palliative or emergency surgery. * Planned for open abdominal surgery or creation of a new stoma. * Transfer to ICU. * Diagnosed with severe heart, liver, kidney or mental system diseases. * Patients with implanted cardiac pacemakers. * Patients currently using or having used in the past month glucagon-like peptide-1 (GLP-1) receptor agonists, dual glucose-dependent insulinotropic polypeptide (GIP) receptor agonists, and sodium-glucose cotransporter-2 (SGLT-2) inhibitors. * Planned to use epidural anesthesia or epidural analgesia. * Presence of local skin lesions, infection at the stimulation site, or obvious skin allergy or severe skin sensitivity to electrodes/adhesive materials. * Participated in other clinical studies within the past 3 months or received acupuncture treatment within the past month. * Other conditions that the investigator considers make the patient unsuitable for participation in this study.
- Indexed under
- Colorectal Cancer