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A randomized controlled clinical study on the effect of moxibustion on the quality of life in patients with gastric cancer

A randomized controlled clinical study on the effect of moxibustion on the quality of life in patients with gastric cancer

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2000004191
Enrollment
Unknown
Registered
2020-12-24
Start date
2019-11-01
Completion date
Unknown
Last updated
2023-02-20

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

Conditions

gastric cancer

Interventions

Sponsors

Hebei University of Chinese Meidicne
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1.Patients who meet the " Chinese Society of Clinical Oncology (CSCO) Guidelines for Diagnosis and Treatment of Gastric Cancer" (2018.V1) diagnosed as gastric cancer by cytology or histopathology; 2.According to the American Joint Committee on Cancer (AJCC) / The Union for International Cancer Control (UICC) gastric cancer TNM staging system (8th edition), patients who with gastric cancer in stage II, III and IV; 3.Patients whose inspection indicators are in line with chemotherapy indications and undergoing in chemotherapy treatment; 4.The patients age from 18 to 70 years old, regardless of gender; 5.KPS score is over 60; 6.The estimated survival time is not less than 3 months through symptoms, signs and other auxiliary examinations; 7.The patients have good compliance, understand the real situation of this study, participate voluntarily, and sign the informed consent.

Exclusion criteria

Exclusion criteria: 1.Patients in perioperative preoperative chemotherapy 2.Pregnant or lactating women; 3..Patients with severe hepatic and renal dysfunction,or combined with severe cardiovascular and cerebrovascular diseases, diabetes, infectious diseases, etc., with obvious bleeding tendency; 4.Patients with poor compliance, or mental disorders cannot cooperate with treatment; 5.Patients have been accepted other therapeutic measures similar to this study, which may interfere with or affect the observation indicators of this trial.

Design outcomes

Secondary

MeasureTime frame
classification criteria table for acute and subacute toxicity of anticancer drugs made by WHO;Tumor Marker: AFP, CEA, CA125, CA153/PSA, CA199;The results of routine blood test and biochemical test;

Primary

MeasureTime frame
the Index of Nausea, Vomiting and Retching;MD Anderson Symptom Inventory - Traditional Chinese Medicine (MDASI-TCM);European organization for research and treatment of cancer quality of life questionair (EORTC QLQ-C30+STO22);Safety Evaluation;

Countries

China

Contacts

Public ContactPan Lijia

College of Acupuncture and Moxibustion, Hebei University of Chinese Meidicne

panlijia369@126.com+86 18032003570

Outcome results

None listed

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