About this trial

This study aims to elucidate the therapeutic efficacy of electroacupuncture in managing chemotherapy-induced gastrointestinal symptom clusters through clinical research. Building upon this foundation, multi-omics analyses will be conducted to investigate the regulatory effects and underlying mechanisms of electroacupuncture on gastrointestinal symptoms. Ultimately, genomic studies will be performed to further clarify the key targets of electroacupuncture intervention, thereby providing high-level evidence-based medical support and theoretical foundations for optimizing electroacupuncture strategies in addressing chemotherapy-induced gastrointestinal symptoms in patients with cancer.

Eligibility criteria

Qualifiers

Pathologically confirmed stage I-III breast cancer;

An Eastern Cooperative Oncology Group Performance Status (ECOG PS) score of 0-1;

Age between 18 and 75 years;

Scheduled to receive highly emetogenic chemotherapy regimens, such as EC (epirubicin + cyclophosphamide) or platinum-based regimens, during the first cycle of neoadjuvant/adjuvant chemotherapy;

Disqualifiers

Patients with advanced-stage cancer;

Those undergoing concurrent chemoradiotherapy;

Individuals with severe impairment of vital organ function who cannot tolerate standard-dose chemotherapy;

Patients with contraindications to acupuncture, such as active skin infections;

Trial design

Treatments tested in this trial

  • electroacupuncture
  • standard quadruple antiemetic therapy
  • sham electroacupuncture
  • standard quadruple antiemetic therapy

Treatment groups

388 Participants
are divided into 2 treatment groups

Locations

1
Qinghai University Affiliated Hospital810000, XiningQinghai, China

Sponsors and collaborators

Jiuda Zhao

Lead sponsor

Affiliated Hospital of Qinghai University

Sponsor institution