Transcutaneous Electrical Acupoint Stimulation for Opioid Consumption After Gastrointestinal Laparoscopic Surgery
Launched by NANFANG HOSPITAL, SOUTHERN MEDICAL UNIVERSITY · Sep 5, 2023
Trial Information
Current as of July 01, 2025
Recruiting
Keywords
ClinConnect Summary
This clinical trial is studying a method called transcutaneous electrical acupoint stimulation (TEAS) to see if it can help reduce the need for opioid pain medication after patients undergo laparoscopic gastrointestinal surgery, which is a type of minimally invasive surgery. In the trial, all participants will receive standard pain relief methods, but those in the experimental group will also receive TEAS, while those in the control group will receive a placebo treatment that does not provide any real stimulation.
To participate in this trial, you need to be at least 18 years old and scheduled for elective laparoscopic gastrointestinal surgery. You should also be in good overall health, with a body mass index (BMI) between 18.5 and 28, and you need to be able to give informed consent. If you have certain conditions like skin infections near the treatment area, severe nerve damage, or if you're part of another clinical trial, you may not be eligible. Participants can expect close monitoring during the study and will be asked to report their pain levels using a simple scale. This study aims to find a safer way to manage pain after surgery and help reduce reliance on opioids.
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- • aged 18 years or older;
- • scheduled for elective laparoscopic gastrointestinal surgery;
- • informed consent;
- • American Society of Anesthesiologists Physical Status Grades I-III;
- • body mass index (BMI) between 18.5 kg/m2 and 28 kg/m2
- Exclusion Criteria:
- • local skin infection, incision or scar near the study acupoints;
- • nerve damage in upper or lower limbs;
- • participation in other clinical trials that influence the evaluation of the results of this study;
- • inability to understand the Visual Analog Scale (VAS) score or disagreeing with the use of patient controlled analgesia;
- • presence of a pacemaker;
- • patients with severe CNS diseases or severe mental disorders;
- • operations requiring enterostomy or converts to laparotomy;
- • patients who need to be transferred to the intensive care unit (ICU) for treatment after surgery.
About Nanfang Hospital, Southern Medical University
Nanfang Hospital, affiliated with Southern Medical University, is a leading medical institution in China renowned for its comprehensive clinical services and commitment to advancing healthcare through research and education. As a clinical trial sponsor, Nanfang Hospital leverages its state-of-the-art facilities and a multidisciplinary team of expert researchers to conduct innovative studies aimed at improving patient outcomes and contributing to the global medical community. The hospital's focus on ethical standards and patient safety ensures that all trials are conducted with the highest level of integrity and scientific rigor.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Guangzhou, Guangdong, China
Patients applied
Trial Officials
Guoxin Li, M.D.,Ph.D.
Principal Investigator
Nanfang Hospital, Southern Medical University
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported