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Electroacupuncture for Gastric Cancer-Related Sarcopenia with Qi-Blood Deficiency: A Clinical Efficacy and Safety Study

Electroacupuncture for Gastric Cancer-Related Sarcopenia with Qi-Blood Deficiency: A Clinical Efficacy and Safety Study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2026000476
Enrollment
Unknown
Registered
2026-03-05
Start date
2026-03-22
Completion date
Unknown
Last updated
2026-03-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Gastric cancer-related sarcopenia

Interventions

Trial group:Electroacupuncture intervention with basic chemotherapy
Control group:Sham electroacupuncture intervention with basic chemotherapy

Sponsors

Yueyang Integrated Traditional Chinese and Western Medicine Hospital affiliated with Shanghai University of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
45 Years to 80 Years

Inclusion criteria

Inclusion criteria: (1) Pathologically diagnosed gastric cancer with a history of gastrectomy, concurrently meeting the diagnostic criteria for sarcopenia; TNM stage II-III; and presenting with the traditional Chinese medicine syndrome pattern of Qi and Blood Deficiency. (2) Scheduled to receive at least 2 cycles of platinum-based chemotherapy in combination with fluoropyrimidine agents, based on the pathological results and individual patient status. (3) Aged between 45 and 80 years (inclusive), regardless of gender. (4) Karnofsky Performance Status (KPS) score = 60, with an estimated life expectancy exceeding 3 months. (5) Mentally clear and cognitively intact, capable of understanding assessment scales and completing questionnaires independently. (6) Voluntary participation with signed informed consent.

Exclusion criteria

Exclusion criteria: (1) Presence of other concurrent malignancies or significant primary diseases affecting the cardiovascular, cerebrovascular, hepatic, renal, endocrine, hematological, or neuropsychiatric systems, or a history of bleeding tendency. (2) Diagnosis of major infectious diseases such as AIDS, Hepatitis B, Hepatitis C, or Syphilis. (3) Receipt of Traditional Chinese Medicine, acupuncture, or other related therapies within 4 weeks prior to enrollment, or participation in other drug clinical trials during the same period; or any history of acupuncture treatment within the past 5 years. (4) Known allergy to acupuncture or severe psychological aversion/fear that would preclude cooperation with the treatment. (5) Chronic alcohol or tobacco dependence. (6) Women who are pregnant or lactating. Patients meeting any of the above criteria will be excluded.

Design outcomes

Primary

MeasureTime frame
Appendicular skeletal muscle mass index;

Secondary

MeasureTime frame
Grip strength;6 meters daily walking speed;Symptom and signs score of Chinese Medicine;EORTC QLQ-C30 (V3.0) Chinese Version.;Nutritional and Hematological Indices (Albumin, Hemoglobin);Inflammatory markers (IL-6, TNF-a, CRP);

Countries

China

Contacts

Public ContactLi Jing

Yueyang Hospital of Integrated Traditional Chinese and Western Medicine, Shanghai University of Traditional Chinese Medicine

LIJINGacu@126.com18930568565

Outcome results

None listed

Source: ITMCTR (via WHO ICTRP) · Data processed: Apr 4, 2026