Peripheral Neuropathy Trial, Recruiting NCT07377279 Sponsor: Sun Yat-Sen Memorial Hospital of Sun Yat-Sen University Condition: Peripheral Neuropathy
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Peripheral Neuropathy Trial, Recruiting

NCT07377279
Recruiting Not Applicable

Who may be able to join

AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI

Who might be able to join this trial:

  • People aged 18 to 70 years old who have signed a consent form to participate
  • People diagnosed with early or intermediate-stage breast cancer (confirmed by tissue testing) that has not come back after previous treatment
  • People whose treatment plan includes a course of chemotherapy using taxane-based drugs (either a 4-cycle or single-cycle plan)
  • People who have not previously had any chemotherapy, immunotherapy, or hormone therapy for breast cancer
  • People whose heart scan (echocardiogram) shows the heart is pumping normally
  • People who are generally able to carry out daily activities with no more than mild limitations (confirm with trial site regarding specific ECOG score requirement)
  • People who have no mental health or thinking difficulties that would prevent them from understanding and completing questionnaires
  • People who have no signs of nerve damage caused by chemotherapy at the start of the trial
  • People whose blood counts and organ function (including liver, kidneys, and blood cells) meet specific healthy ranges set by the trial
  • Women who could become pregnant must agree to use reliable contraception starting 7 days before the first treatment through 24 weeks after treatment ends, and must have a negative blood pregnancy test within 7 days before the first treatment

Who may not be able to join:

  • People with active infections, skin sores on the hands or feet, or any medical reason that prevents them from receiving chemotherapy, acupuncture, or compression therapy
  • People who have previously been treated with certain nerve-affecting chemotherapy drugs such as taxanes, oxaliplatin, platinum-based drugs, or vincristine
  • People who have had acupuncture treatment for any reason within the past month
  • People with conditions that can already cause nerve damage or similar symptoms, such as diabetes, alcoholism, kidney disease, autoimmune conditions, rheumatoid arthritis, neck spine problems, severe mental illness, or severe physical trauma
  • People with Raynaud's syndrome, sensitivity to cold, poor blood circulation in the limbs, or hand-foot syndrome
  • People currently taking medications that could hide nerve damage symptoms, such as certain antidepressants (SSRIs, SNRIs, tricyclics) or B-complex vitamins
  • People who have swelling caused by lymph fluid (lymphedema) in areas where acupuncture would be applied
  • People who have a fear of electroacupuncture or an allergy to stainless steel needles
  • People with serious non-cancer health conditions that may make it difficult to follow the trial treatment plan
  • People who are currently receiving other cancer treatments or participating in another clinical trial
  • People with dementia, cognitive difficulties, or psychiatric conditions that affect their ability to understand and give informed consent
  • People with a known allergy or medical reason that prevents them from undergoing the trial procedures
  • People with serious or uncontrolled heart problems, including moderate-to-severe heart failure, unstable chest pain, a heart attack within the past year, or significant heart rhythm problems requiring treatment
  • People who have a cardiac pacemaker
  • People with known bleeding or clotting disorders, such as haemophilia, low platelet counts, or other conditions affecting the blood's ability to clot

Important: Always verify eligibility with the trial site directly before applying.

Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 28 July 2026
This study is not part of the standard drug-approval phase pathway (for example an observational, device, behavioural, or registry study), so a phase success rate does not apply.

Contact this trial

Phone: 86-13922272706

Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.

GP referral letter

Print a one-page summary to share with your doctor.

Trial details

Status
Recruiting
Phase
Not Applicable
Sponsor
Sun Yat-Sen Memorial Hospital of Sun Yat-Sen University
Registry
ClinicalTrials.gov
Start date
1 September 2025
Est. completion
30 September 2028

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Incidence of grade ≥2 CIPN at 12 weeks after the initiation of chemotherapy

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 28 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov