Clin2
NCT05841186Possibly a fitRecruiting

Timing Pegfilgrastim Dose in Breast Cancer Patients

PegfilgrastimBone PainChemotherapyBreast CancerPatient-reported OutcomesQuality of Life

Part of Cancer, Skin clinical trials.

This study looks at whether changing the timing of pegfilgrastim (a medicine used to help prevent low white blood cell counts during chemotherapy) affects outcomes in people with primary breast cancer. It may help your care team choose the best dosing schedule for you during treatment.

Summary written for real people, not researchers, by Clin2.

Phase
N/A
Enrollment
156 people
Ages
18 years to 70 years
Study type
Interventional

Who can take part

  • You are age 18 to 70
  • You have confirmed primary breast cancer (from a lab test of tissue or cells)
  • You can receive your chemotherapy exactly as planned in the study
  • You can read and understand Chinese and complete questionnaires on your own
  • You can sign consent to join the study
  • You do not regularly take prescription or over-the-counter medicines for ongoing chronic pain

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

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