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Search / Trial NCT07044414

Effectiveness of Manual Acupuncture for Head and Neck Cancer Patients Undergoing Chemoradiation

Launched by INDONESIA UNIVERSITY · Jun 23, 2025

Trial Information

Current as of July 28, 2025

Not yet recruiting

Keywords

ClinConnect Summary

This clinical trial is studying whether manual acupuncture can help patients with head and neck cancer who are receiving combined chemotherapy and radiation treatment (called chemoradiation). The researchers want to see if acupuncture can improve patients’ white blood cell counts, which are important for fighting infections, and reduce cancer-related tiredness (fatigue). They also want to find out if acupuncture can improve overall quality of life during this tough treatment.

Adults with head and neck cancer who have finished initial chemotherapy and are starting chemoradiation may be eligible to join. To participate, patients need to be generally healthy enough, with good mental function and normal oxygen levels, and not have serious other illnesses or blood problems. Participants will be randomly assigned to receive either real acupuncture or a fake version (sham acupuncture) three times a week for seven weeks. The acupuncture will target specific points on the body, and patients will be checked weekly for changes in blood counts, fatigue levels, and quality of life. This study is not yet open for enrollment but aims to find out if acupuncture can be a helpful support during cancer treatment.

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • Subjects diagnosed with head and neck cancer (HNC) based on histopathological examination, who have completed induction chemotherapy and are scheduled to undergo radiotherapy.
  • Subjects aged ≥18 years.
  • Subjects willing to participate in this study and provide written informed consent.
  • Subjects with a Mini Mental State Examination (MMSE) score ≥24.
  • Subjects with oxygen saturation ≥95% on room air.
  • Subjects with stage III or IVA cancer.
  • Subjects receiving a radiation dose of 66-70 Gy.
  • Exclusion Criteria:
  • Subjects with severe comorbidities such as chronic kidney failure, metastatic liver cirrhosis, or heart disease.
  • Subjects currently undergoing other therapies that may affect leukocyte counts, such as immunomodulatory therapy or high-dose corticosteroid use.
  • Subjects who are still smoking or consuming alcohol.
  • Subjects with blood clotting disorders or those currently taking anticoagulants, confirmed by laboratory results: neutrophils \<1,000/mm³, platelets \<25,000/mm³, INR \>2.0, or partial thromboplastin time \>20 seconds.
  • Pregnant or breastfeeding women.

About Indonesia University

Indonesia University is a leading academic institution dedicated to advancing healthcare through rigorous clinical research. As a trial sponsor, the university leverages its extensive expertise in medical science and collaboration with top-tier researchers to design and implement innovative clinical trials. Committed to ethical standards and patient safety, Indonesia University aims to contribute to the global body of knowledge in medicine, enhance therapeutic options, and improve health outcomes for diverse populations. Through its comprehensive approach, the university fosters an environment of scientific inquiry and collaboration, driving progress in clinical research and education.

Locations

Jakarta Pusat, Dki Jakarta, Indonesia

Patients applied

0 patients applied

Trial Officials

KPEK FKUI-RSCM

Principal Investigator

The Health Research Ethics Commitee of Faculty Medicine

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported