Peripheral Neuropathy 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 have willingly agreed to take part and signed a consent form.
- You are between 18 and 75 years old (any gender).
- You are generally well enough to carry out daily activities with little to no limitation (confirm with trial site).
- Your doctor has determined that a chemotherapy drug called albumin-paclitaxel is an appropriate treatment for you.
- Your heart, lungs, liver, kidneys, and blood clotting are all working at a basically normal level.
Who may not be able to join:
- You have previously received chemotherapy treatment.
- You have been diagnosed with nerve damage or a nerve condition affecting your hands, feet, or other parts of the body (known as peripheral neuropathy).
- You have been diagnosed with certain other health conditions alongside your current illness, such as diabetes (confirm with trial site for full list of conditions).
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.
Contact this trial
Phone: (022)65150123-8212
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
Where this trial is recruiting
Primary endpoints
CIPN-related symptoms, as assessed by changes in tactile sensitivity at pretreatment baseline CIPN incidence.The Patient Neurotoxicity Questionnaire (PNQ) was used to assess and grade the incidence and severity of CIPN.
Can't join this trial?
Data last synced from ClinicalTrials.gov: 12 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.