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Clinical Trials in China / NCT06931743
Recruiting Not applicable

The Application of Electrical Stimulation in Postoperative Pain Management of Thyroid Surgery

NCT06931743 · tracked via the Priya Life Science China tracker
Sponsor
Xiaonan Huang
Phase
Not applicable
Started
2025-04-30
Last updated
2026-08-19

Condition(s) studied

Thyroid SurgeryElectrical StimulationThyroid Carcinoma

Investigational drug(s) / intervention(s)

CMNS6-1 Electronic Acupuncture Therapeutic ApparatusCMNS6-1 Electronic Acupuncture Therapeutic Apparatus

CMNS6-1 Electronic Acupuncture Therapeutic Apparatus: 1. The time selection of acupoint treatment is to return to the ward immediately,2 and 4 hours after surgery; 2. Time of each stimulation: 30min; 3. Acupoint extraction: According to the theory of wrist and ankle acupuncture and the location of pain, the upper 1 area (the ulnar margin on the little finger side and the depression of the flexor carpi ulnaris tendon) and the upper 2 area (between the palmaris longus tendon and the flexor carpi radialis on both sides) on the affected side (bilateral for total thyroidectomy) were selected as the intervention site, and the upper and lower parallel electrodes were placed in each area, and a total of 4 electrodes (8 electrodes on both sides) were placed. 4. The parameter setting of the equipment: the frequency is set to 2Hz, the pulse width is set to 250μs, continuous wave is used, and the current intensity is the maximum tolerance of the subject's small pain threshold for 30min.

CMNS6-1 Electronic Acupuncture Therapeutic Apparatus: 1. The time selection of acupoint treatment is to return to the ward immediately,2 and 4 hours after surgery; 2. Time of each stimulation: 30min; 3. Acupoint extraction: According to the theory of wrist and ankle acupuncture and the location of pain, the upper 1 area (the ulnar margin on the little finger side and the depression of the flexor carpi ulnaris tendon) and the upper 2 area (between the palmaris longus tendon and the flexor carpi radialis on both sides) on the affected side (bilateral for total thyroidectomy) were selected as the intervention site, and the upper and lower parallel electrodes were placed in each area, and a total of 4 electrodes (8 electrodes on both sides) were placed. (4)30 minutes of ineffective microcurrent stimulation.

Study summary

Post-thyroidectomy pain is a prevalent early postoperative complication. While pharmacological agents remain the mainstay of analgesia, their clinical application is constrained by adverse effects including nausea, respiratory depression, and gastrointestinal disturbances. Transcutaneous electrical nerve stimulation based on wrist-ankle acupuncture theory (TENS-WAA) is a non-invasive analgesic modality that has demonstrated preliminary benefits in multiple pain scenarios. Nevertheless, robust evidence for its efficacy in post-thyroidectomy pain management is still lacking, limited by single-center designs and small sample sizes in existing studies.

This trial aims to evaluate the efficacy and safety of TENS-WAA for pain control after thyroidectomy. The findings are expected to support a standardized non-pharmacological analgesic option as an adjunct to multimodal postoperative pain regimens, aligning with Enhanced Recovery After Surgery (ERAS) principles.

Eligibility

Sex
ALL
Min age
18 Years
Max age
Healthy volunteers
No
1. Inclusion Criteria: * Be over 18 years of age; * The operation time is less than 4 hours; * Postoperative VAS pain score ≥3 points ; * Clear consciousness, able to answer questions accurately, free speech, no hearing impairment; * Informed consent 2. Exclusion Criteria: * Neck or thyroid surgery within the past ten years; * Menstruating, pregnant and lactating females;Those who are not satisfied with blood glucose control; * Skin injury or allergy; skin ulceration; * Past history of psychiatric disorder that met the diagnostic criteria of Diagnostic and Manual of Mental Disorders, DSM-IV; * Upper respiratory tract infection within 2 weeks before surgery; * History of implantation of pace or defibrillator; * Allergic to gel or intolerant to electrical stimulation; * History of chronic pain, pain VAS score 1 at the examination; * Use of sedative analgesic drugs for a long time or within 24 hours; * Particip in other clinical trials in the past 4 weeks.

Primary outcome measure(s)

Trial sites (3)

FacilityCityRegionStatus
the Specialised Medical Centre of the Chinese People's Liberation Army Navy Shanghai Changning District Recruiting
Changzheng Hospital Affiliated to the Naval Medical University Shanghai Huangpu District Recruiting
Changhai Hospital Affiliated to the Naval Medical University Shanghai Yangpu District Recruiting

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06931743 on ClinicalTrials.gov ↗ ← All trials in China