Breast Cancer Trial, Recruiting NCT06602167 Sponsor: Affiliated Hospital of Qinghai University Condition: Breast Cancer
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Breast Cancer Trial, Recruiting

NCT06602167
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:

  • 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.

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 2 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.

GP referral letter

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

Trial details

Status
Recruiting
Phase
Not Applicable
Sponsor
Affiliated Hospital of Qinghai University
Registry
ClinicalTrials.gov
Start date
8 October 2024
Est. completion
30 July 2027

Where this trial is recruiting

🇨🇳 China

Primary endpoints

HFS incidence rate (Compare the difference between the two groups)

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: 2 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