Clinical Trials Directory

Trials / Not Yet Recruiting

Not Yet RecruitingNCT07133620

the Effect of Transcutaneous Electrical Acupoint Stimulation on Postoperative Gastrointestinal Dysfunction After Urological Laparoscopic Surgery

The Effect of Transcutaneous Electrical Acupoint Stimulation on Postoperative Gastrointestinal Dysfunction After Urological Laparoscopic Surgery

Status
Not Yet Recruiting
Phase
N/A
Study type
Interventional
Enrollment
112 (estimated)
Sponsor
The First Affiliated Hospital of Xiamen University · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Accepted

Summary

The purpose of this clinical trial is to understand the effect of percutaneous acupoint electrical stimulation on postoperative gastrointestinal dysfunction. It will also investigate the safety of percutaneous acupoint electrical stimulation. The main questions that this trial aims to answer are: Can percutaneous acupoint electrical stimulation alleviate postoperative gastrointestinal dysfunction? Through which mechanisms do they function? Participants will: Preoperatively, patients were either given or not given percutaneous acupoint electrical stimulation. Record their symptoms and biological indicators within 5 days after the operation.

Conditions

Interventions

TypeNameDescription
DEVICETranscutaneous electrical acupoint stimulationBefore the operation, the patient received transcutaneous electrical acupoint stimulation (TEAS) at bilateral Zusanli (ST 36), Neiguan (PC 6), and Ciliao (BL 32) acupoints with sterilized electrode patches. The stimulation intensity and current intensity that gave the patient an effective pricking sensation ("Qi arrival") were maintained for 30 minutes. The stimulation method in the post-anesthesia care unit (PACU) was consistent with that before the operation.
DEVICESham transcutaneous Electrical Acupoint StimulationBefore the operation, disinfection patches with electrodes were applied to Zusanli (ST 36), Neiguan (PC 6), and Ciliao (BL 32) acupointst, but no electrical stimulation was conducted. The stimulation method in the post-anesthesia care unit (PACU) was the same as that before the operation.

Timeline

Start date
2025-09-01
Primary completion
2026-09-01
Completion
2026-09-30
First posted
2025-08-21
Last updated
2025-08-21

Source: ClinicalTrials.gov record NCT07133620. Inclusion in this directory is not an endorsement.