Clinical trial Recruiting at 1 site Interventional Ages 18 and up Women only

Acupuncture to reduce chemotherapy-related nerve pain after gynecologic cancer

Official title: The Use of Acupuncture to Reduce Chemotherapy Induced Peripheral Neuropathy (CIPN) in Gynaecological Cancer Patients - A Pilot Randomised Controlled Trial

Run by The University of Hong Kong · NCT06769061 · Data updated 2026-11-12

This pilot will try acupuncture to see if it reduces chemotherapy-caused nerve pain (peripheral neuropathy) in people treated for gynecological cancers with carboplatin and paclitaxel.

More Chemotherapy-induced Peripheral Neuropathy trials

Quick facts

Study typeInterventional
Ages18 Years and up
SexWomen only
Enrollment75 (estimated)
SponsorThe University of Hong Kong
Academic / other
Drugs / interventionschemotherapy
Locations1 site (Hong Kong)
StatusRecruiting
StartedFebruary 12, 2025
Main results expectedJune 2027
Study endsDecember 2027
Registry record updatedFebruary 25, 2026
Trial IDNCT06769061 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Adults (≥18) with ovarian, endometrial, or cervical cancer who completed at least six cycles of carboplatin or cisplatin plus paclitaxel at least three months ago, have PNQ grade C or higher, ECOG 0–2, and life expectancy over six months.

Probably not a fit

Patients with pre-existing non-chemotherapy neuropathy, ongoing chemotherapy, bleeding or clotting disorders, platelet counts below 50, pacemakers, recent acupuncture, or on routine anticoagulants are excluded and unlikely to benefit from this trial.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This is a single-center, pilot, randomized controlled trial at Queen Mary Hospital enrolling gynecological cancer patients with chemotherapy-induced peripheral neuropathy after platinum-plus-paclitaxel treatment. Participants are randomized 1:1:1 to electroacupuncture, sham acupuncture, or a waiting-list usual-care control, with blinding of patients and assessors between the real and sham acupuncture arms. The trial uses standardized screening (including PNQ score ≥ C and bloodwork) and delivers 12 acupuncture sessions, with sham and wait-list participants offered active treatment after study completion. Results will inform feasibility and provide preliminary effectiveness data to plan a larger multicenter trial.

Why it matters

Potential benefit: If successful, acupuncture could reduce numbness, tingling, and pain from chemotherapy and improve daily function and quality of life for affected patients.

How similar studies have gone: Small randomized and pilot studies have suggested acupuncture may help chemotherapy-induced peripheral neuropathy, but evidence is limited and larger trials are still needed.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Age 18 or above
* Diagnosis of uterine (endometrial) cancer, ovarian cancer and cervical cancer
* ECOG=0-2
* Life expectancy of \> 6 months
* Completed at least 6 cycles of carboplatin or cisplatin chemotherapy together with paclitaxel at least 3 months before joining the study
* Able to read and understand the questionnaires
* PNQ score of C or above

Exclusion Criteria:

* Bleeding tendency
* Abnormal clotting profile
* Platelet lower than 50
* Received acupuncture in the past
* Currently receiving chemotherapy treatment
* Known neurological disorders or pre-existing neuropathy unrelated to chemotherapy
* Routinely take aspirin or any anticoagulant drugs
* Having active skin infection
* With pacemaker

Where it's running

  • Department of Obstetrics and Gynaecology
    Hong Kong, Hong Kong
    Recruiting

Study contacts

  • Principal investigator: Karen Kar Loen Prof CHAN, MBBChir (Cantab); MD (HK) — Department of Obstetrics and Gynaecology, the University of Hong Kong
  • Study coordinator: Karen Kar Loen CHAN, MBBChir (Cantab); MD (HK)
  • Email: kklchan@hku.hk
  • Phone: 852-2255 4265

Similar studies

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.