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Study identifier: NCT06524609 Synced from ClinicalTrials.gov · July 28, 2026
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EGCG for the Prevention and Treatment of TIPN

Condition: Chemotherapy-induced Peripheral Neuropathy  ·  Sponsor: Han Xi Zhao

PhasePhase 1/Phase 2
Planned participants36
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

Patients treated with paclitaxel analogs and experiencing Taxane-induced peripheral neurotoxicity (TIPN) of degree I or higher were treated with EGCG solution. The safety of topical EGCG solution for the treatment of TIPN and the optimal drug concentration were also verified by a phase I trial. The efficacy and safety of the optimal EGCG concentration obtained in the phase I trial were further analyzed in a randomized controlled phase II trial. Meanwhile, the predictive molecules of TIPN efficacy were initially explored by detecting patients' hematological related indexes. The optimal dose concentration, safety and efficacy of EGCG to ameliorate the neurotoxicity caused by paclitaxel-related drugs were clarified.

This description comes directly from the study's public registry record.

Talk to the study team

Hanxi Zhao, Dr.  ·  86-053167626995  ·  zhx7152028@126.com

Always discuss trial participation with your own doctor first.

Locations (1)

Shandong First Medical University Affiliated Cancer Hospital (Shandong Academy of Medical Sciences)Jinan, Shandong, ChinaRecruiting

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Source record: clinicaltrials.gov/study/NCT06524609