Clinical trial · Interventional
Effect of Acupuncture for QoL in Gastric Cancer Patients Undergoing Adjuvant Chemotherapy: a Pilot Study
Effect of Acupuncture for Quality of Life in Patients With Gastric Cancer Undergoing Adjuvant Chemotherapy: a Pilot Study
NCT03753399CI-TRIAL-00051909completedN/AClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
This is a pilot study evaluating the efficacy of acupuncture on quality of life in gastric cancer patients undergoing postoperative adjuvant chemotherapy. Enrolled participates will randomly receive high-dose acupuncture, low-dose acupuncture or none-acupuncture during the first 3 cycles of adjuvant chemotherapy after resection.
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Stomach Neoplasms | Gastric Neoplasm | ALIAS | 0.90 |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| acupuncture | Procedure | — | UNRESOLVED |
Design
Arms and outcomes
Arms (3)
- type
- EXPERIMENTAL
- label
- High-dose acupuncture
- description
- Acupuncture for 7 times every 3 weeks (a cycle of chemotherapy) for 9 weeks
- interventionNames
- Procedure: acupuncture
- type
- EXPERIMENTAL
- label
- Low-dose acupuncture
- description
- Acupuncture for 3 times every 3 weeks (a cycle of chemotherapy) for 9 weeks
- interventionNames
- Procedure: acupuncture
- type
- NO_INTERVENTION
- label
- Usual care
- description
- Chemotherapy without acupuncture
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
- Maximum age
- 75 Years
Show eligibility criteria text
Inclusion Criteria: * 1.Pathologically diagnosed with gastric cancer or esophagogastric junction cancer after R0 resection and D2 lymph node dissection; * 2.Pathological stage II or stage III; * 3.Without tumor recurrence confirmed by image examination; * 4.No chemotherapy after surgery, planning to accept at least 3 cycles of adjuvant chemotherapy; * 5.Age:18\~75 years old; * 6.ECOG score≤ 2; * 7\. Normal organs function, including: 7.1 Bone marrow function: absolute neutrophil count (ANC)≥1.5×10e9/L, platelet (PLT)≥100×10e9/L,hemoglobin (Hb)≥90g/L; 7.2 Kidney function: Serum creatinine (Scr)≤1.5mg/dl(133μmol/L), or creatinine clearance rate (Ccr)≥60ml/min; 7.3 Liver function: Total bilirubin (TB)≤1.5×upper limit of normal value (ULN), Alanine transaminase (ALT)≤2.5×ULN, Aspartate transaminase (AST)≤2.5×ULN; * 8\. Can understand the study well and finish the questionnaires in this study; * 9\. With the written informed consent. Exclusion Criteria: * 1\. Can not finish the baseline assessment; * 2\. Needle phobia; * 3\. Currently diagnosed with psychiatric disorder (e.g., severe depression, obsessive-compulsive disorder, or schizophrenia); * 4\. History of autoimmune diseases, hematological diseases or organ transplantation, or long term use of hormones or immunosuppressors; * 5\. Implanted with heart pacemaker; * 6\. Has accepted neoadjuvant radiotherapy before surgery; * 7\. Planning to accept adjuvant radiotherapy after surgery; * 8\. With active infection; * 9\. Acupuncture treatment within the previous 6 weeks; * 10.Pregnant or lactating women.
References
Publications (0)
Data not yet available
No reference posted for this study.