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The Efficacy of Electrical Acupoint Stimulation Based on Syndrome Differentiation and Treatment on Chemotherapy-Induced Myelosuppression in Patients with Oral and Maxillofacial Tumors

The Efficacy of Electrical Acupoint Stimulation Based on Syndrome Differentiation and Treatment on Chemotherapy-Induced Myelosuppression in Patients with Oral and Maxillofacial Tumors

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600116779
Enrollment
Unknown
Registered
2026-01-14
Start date
2025-11-14
Completion date
Unknown
Last updated
2026-01-27

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

Conditions

Oral and Maxillofacial Tumor

Interventions

Interventionall group:Interventions were carried out during the patients' second and third chemotherapy hospitalizations. On the 1st, 2nd, and 3rd days of hospitalization, twice a day, 30 minutes each
Control group:During the chemotherapy cycle, patients will be hospitalized for chemotherapy. In addition to receiving routine care and health guidance, no other interventions to promote hematopoiesis

Sponsors

Ninth People's Hospital Affiliated to Shanghai Jiao Tong University School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 79 Years

Inclusion criteria

Inclusion criteria: 1.Comply with the diagnostic criteria for oral and oropharyngeal cancer pathology diagnosis standards set by the Chinese Stomatological Association and the 2022 Head and Neck Tumor Diagnosis and Treatment Guidelines by the Chinese Society of Clinical Oncology (CSCO), and have a definitive histopathological diagnosis of oral and maxillofacial tumors; 2. Be newly diagnosed and receiving first-line platinum-based chemotherapy; 3.Be aged 18 to 79 years old; 4.Have an Eastern Cooperative Oncology Group Performance Status (ECOG) score of =3 months; 5.Have no myelosuppression prior to chemotherapy; 6.Have no severe organic diseases of the heart, liver, kidneys, or other organs; 7. Have no psychiatric diseases or cognitive impairments, and be able to understand and comply with the study requirements; 8.Provide informed consent.

Exclusion criteria

Exclusion criteria: 1. Patients with hematological diseases or autoimmune diseases that significantly affect the hematopoietic system of the bone marrow; 2.Patients who cannot tolerate the drugs used in this study or the electrostimulation therapy, such as severe skin damage or infection; 3.Pregnant or breastfeeding women; 4. Other situations deemed by the investigator as unsuitable for participation in this study.

Design outcomes

Primary

MeasureTime frame
Platelet count;

Secondary

MeasureTime frame
General demographic data:Gender, age, educational level, marital status, living situation, BMI, etc.;General clinical data:Tumor location, pathological type, disease course stage, chemotherapy regimen, comorbidities, current chemotherapy cycle, etc.;Quality of life;Other blood routine counts apart from platelet count, including post-intervention white blood cell count, absolute neutrophil count, red blood cell count, and hemoglobin concentration.;

Countries

China

Contacts

Public ContactHou Lili

Ninth People's Hospital Affiliated to Shanghai Jiao Tong University School of Medicine

pisces_liz@163.com+86 138 1603 3620

Outcome results

None listed

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