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Needles vs. cancer: acupuncture may supercharge immunotherapy

NCT ID NCT06461338

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 This study
Running, but no longer taking on new participants.
Completed
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 27, 2026 · Last updated Jun 27, 2026

Summary

This study tests whether adding acupuncture to standard immunotherapy and chemotherapy helps people with advanced non-small cell lung cancer. Sixty participants will receive either real or sham acupuncture alongside their first four treatment cycles. The goal is to see if acupuncture can improve how well the cancer responds and extend survival.

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

About 60 people

The number the study aims to enrol. It can still change while the study runs.

Started

Aug 2024

Expected to finish

Sep 2026

An estimate. End dates often move.

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: 1. Has a histologically-confirmed or cytologically confirmed diagnosis of stage IIIB or IV NSCLC. 2. PD-L1 TPS\<50% 3. EGFR/ALK wild-type 4. Has not received prior systemic treatment for advanced NSCLC. For patients who received preoperative neoadjuvant chemotherapy or postoperative adjuvant chemotherapy or radical chemoradiotherapy, if the disease progresses occurred one six months after the last treatment, they can be enrolled. Patients who received targeted therapy or immunotherapy can not be enrolled. 5. Has a performance status of 0-2 on the Eastern Cooperative Oncology Group (ECOG) Performance Status. 6. Age≥18 years 7. Has a life expectancy of at least 3 months 8. Has measurable disease 9. Has adequate organ function 10. Voluntarily enrolled into the study, sign the informed consent form and have good compliance Exclusion Criteria: 1. Unable to complete baseline assessments 2. Expected to receive radiotherapy within the next 4 cycles 3. With a combination of serious primary diseases of the heart, cerebrovascular, hepatic, renal, and hematopoietic systems 4. With dementia, neurological disorders, mental retardation, or language impairment, and pregnant or breastfeeding women 5. Combined autoimmune diseases, hematologic disorders, or long-term use of hormones or immunosuppressive drugs 6. Combined with a primary tumor from other sites 7. Had participated in any other clinical trial within the prior 3 months 8. Has known history of Human Immunodeficiency Virus (HIV) or solid organ transplantation 9. With legal incapacity 10. With skin breakdown at the acupuncture point that interferes with treatment 11. With a pacemaker 12. With a fear of acupuncture 13. Had received acupuncture treatment within 6 weeks 14. Has known active Hepatitis B 15. Has interstitial lung disease or a history of pneumonitis that required oral of IV glucocorticoids to assist with management 16. Has fever (\>38°C) or clinically significant infection within 1 week prior to enrolment 17. Has active tuberculosis or indications of severe or uncontrolled systemic diseases 18. With a bleeding tendency, and receiving thrombolytics or anticoagulants

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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

  • Guangdong Provincial Hospital of Chinese Medicine

    Guangzhou, Guangdong, 510120, China

  • Jiangsu Provincial Hospital of Chinese Medicine

    Nanjing, Jiangsu, 210000, China

  • The First Affiliated Hospital of Guangzhou University of Chinese Medicine.

    Guangzhou, Guangdong, 510000, China

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