Breast Cancer Trial, Recruiting
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:
- You are willing and able to sign a consent form agreeing to take part
- You are 18 years old or older (any gender)
- You have been diagnosed with gastrointestinal cancer or breast cancer (confirmed by a lab/pathology test) and are about to receive the chemotherapy drug capecitabine for the first time
- Your general health and ability to carry out daily activities meets a certain standard (rated 0–2 on a standard scale used by doctors — confirm with trial site)
- You are receiving capecitabine as part of palliative or adjuvant chemotherapy (either alone or combined with other drugs), at a minimum daily dose of 2000 mg/m² (confirm with trial site)
- Your doctors expect you to live for at least 3 more months
- Your blood test results are within acceptable ranges — including healthy levels of platelets, white blood cells, and hemoglobin, and your liver and kidneys are functioning normally
- You are using adequate contraception if applicable
Who may not be able to join:
- You have previously been treated with capecitabine, liposomal doxorubicin, or certain other targeted therapy drugs (such as sorafenib, sunitinib, or apatinib) that can cause a side effect called hand-foot syndrome
- Your starting dose of capecitabine is below a certain level (less than 800 mg/m² — confirm with trial site)
- You have had radiation therapy or surgery within the 4 weeks before the trial treatment begins
- You have a skin condition that could affect the trial results
- You have a known problem with drug or alcohol misuse
- You are pregnant or currently breastfeeding
- You are already taking part in another clinical trial and have received an experimental drug within the last 30 days before the start of this trial's treatment
- You are known to be afraid of electroacupuncture (a type of needle-based treatment used in this trial), or you are allergic to stainless steel needles or any ingredient in capecitabine
- You are currently receiving acupuncture or moxibustion treatment, or you have lymph fluid build-up (lymphedema) in the area where acupuncture needles would be placed
- You still have side effects from previous chemotherapy or radiotherapy that have not improved to a mild level (grade 2 or below), except for certain stable nerve-related symptoms
- You have any unresolved skin side effects from previous chemotherapy or radiotherapy (hair loss is an exception to this rule)
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.
GP referral letter
Print a one-page summary to share with your doctor.
Trial details
Where this trial is recruiting
Primary endpoints
HFS incidence rate (Compare the difference between the two groups)
Can't join this trial?
Data last synced from ClinicalTrials.gov: 2 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.