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Acupuncture needles may boost blood counts and ease fatigue in cancer patients

NCT ID NCT07044414

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed This study
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 24, 2026 · Last updated Jun 27, 2026 · Updated 1 time

Summary

This study tested whether manual acupuncture, compared to a sham (fake) version, could improve white blood cell counts and reduce fatigue in 34 head and neck cancer patients undergoing chemoradiation. Participants received 21 sessions over seven weeks at specific body points. The goal was to see if this gentle therapy could help manage common side effects of cancer treatment.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
manual acupuncture
What this could lead to
If it works, this could offer a simple, drug-free way to help head and neck cancer patients feel less tired and keep their white blood cell counts up during chemoradiation.
What could go wrong
This is a small, completed trial with only 34 participants. The results may not apply to everyone, and the benefit over sham acupuncture could be small or absent.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Phase

Not a phased trial

Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.

Participants

34 people

The number who actually took part.

Started

Sep 2025

Finished

Dec 2025

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Ages

18 years and older

Sex

Anyone

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

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.

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Conditions

The condition(s) this trial relates to.

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Contacts and locations

Locations

  • Universitas Indonesia

    Jakarta Pusat, DKI Jakarta, 10430, Indonesia

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