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NCT06024200

Transcutaneous Electrical Acupoint Stimulation for Opioid Consumption After Gastrointestinal Laparoscopic Surgery

Status unknown NA Last updated 11 September 2023
What this trial tests

NA trial testing transcutaneous electrical acupoint stimulation in Transcutaneous Electrical Acupoint Stimulation in 128 participants. Status unknown.

Timeline
2 June 2023
Primary endpoint
30 October 2023
30 January 2024

Quick facts

Lead sponsorNanfang Hospital, Southern Medical University
PhaseNA
StatusStatus unknown
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingtriple
Primary purposetreatment
Enrollment128
Start date2 June 2023
Primary completion30 October 2023
Estimated completion30 January 2024
Sites1 location across China

Drugs / interventions tested

Conditions studied

Sponsor

Nanfang Hospital, Southern Medical University

Who can join

18 and older, any sex, with Transcutaneous Electrical Acupoint Stimulation. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The goal of this clinical trial is to evaluate the effect of whole-process transcutaneous electrical acupoint stimulation on opioid consumption after gastrointestinal laparoscopic surgery. All subjects received conventional multimodal analgesia. On this basis, the experimental group received whole-process transcutaneous electrical acupoint stimulation, while the control group received corresponding false stimulation.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other trials of transcutaneous electrical acupoint stimulation

Trials testing the same drug.

Other Nanfang Hospital, Southern Medical University trials

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06024200.

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