Clinical Trial

TEAS Combined With Triple Antiemetic Drugs to Prevent PONV in High-Risk Patients

Recruiting
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Summary
The goal of this clinical trial is to evaluate the effects of transcutaneous electrical acupoint stimulation (TEAS) combined with triple antiemetics for postoperative nausea and vomiting (PONV) in high-risk patients. The primary question it seeks to answer is: Does TEAS combined with triple antiemetics further reduce the incidence of PONV in high-risk subjects? Researchers will compare active TEAS with sham stimulation to determine whether the addition of TEAS to dexamethasone, palonosetron, and droperidol lowers the PONV rate beyond that achieved by the triple-drug prophylaxis alone.
Trial Details
NCT Number NCT07480785
Lead Sponsor Zhejiang University
Collaborators: Jinhua Central Hospital, Huzhou Central Hospital, The First People's Hospital of Huzhou
Conditions Uterine Fibroids (Leiomyoma), Ovarian Tumors, Gallstones
Enrollment 780 participants
Start Date 2026-01-16
Primary Completion 2027-10-31 (estimated)
Study Completion 2027-10-31 (estimated)
Updated on ClinicalTrials.gov 2026-03-18