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Effect of transcutaneous acupoint electrical stimulation on taste disturbance after radiotherapy in patients with oral malignancies

Effectiveness of transcutaneous electrical acupoint stimulation for prevention of taste disturbance after radiotherapy in patients with oral malignancies: a pilot study

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2200006767
Enrollment
Unknown
Registered
2022-11-11
Start date
2022-11-15
Completion date
Unknown
Last updated
2023-02-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Oral malignancies

Interventions

Low frequency group:usual care + transcutaneous electrical acupoint stimulation intervention, Intervention 3 times a week
Control group:usual care
High Frequency Group:usual care + transcutaneous electrical acupoint stimulation intervention, intervention after each radiotherapy treatment

Sponsors

Shanghai Ninth People's Hospital, Affiliated to Shanghai Jiaotong University, School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: (1) Patients aged 18 years or older who have been diagnosed by the hospital pathology department as having oral malignancies and undergoing radiation therapy. (2) Initial radiotherapy and the irradiation field includes the tongue. (3) Karnofsky (KPS) functional status score = 50; and no serious organic damage to heart, liver, brain, kidney, etc. (4) Patients who participate voluntarily, are conscious, can communicate normally, and have no mental illness or cognitive impairment.

Exclusion criteria

Exclusion criteria: (1) Patients with total tongue removal. (2) Use of drugs that affect gustatory function during radiotherapy (e.g., the cytoprotective agent amphotericin, the saliva-increasing drug pilocarpine). (3) Patients with known or suspected allergy to experimentally relevant materials. (4) Patients with skin breakdown or edema at the selected acupuncture point. (5) Patients with psychiatric disorders and pregnant women.

Design outcomes

Primary

MeasureTime frame
Taste threshold;

Secondary

MeasureTime frame
general comfort questionnaire, GCQ;VAS;QLQH&N35;BMI;

Countries

China

Contacts

Public ContactLili Hou

Shanghai Ninth People's Hospital, Affiliated to Shanghai Jiaotong University, School of Medicine

Pisces_liz@163.com13816033620

Outcome results

None listed

Source: ITMCTR (via WHO ICTRP) · Data processed: Feb 4, 2026