ISRCTN10119971
Completed
Not Applicable
Acupuncture for prevention and treatment of cancer-related fatigue during chemotherapy: a study protocol for a multicenter, randomized, controlled clinical trial
Beijing Municipal Administration of Hospitals0 sites112 target enrollmentMarch 24, 2015
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Cancer-related fatigue
- Sponsor
- Beijing Municipal Administration of Hospitals
- Enrollment
- 112
- Status
- Completed
- Last Updated
- 10 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •1\. Patients with a definite pathologic diagnosis of breast cancer or lung cancer who had completed chemotherapy and/or radiotherapy at least 3 months, or never received chemotherapy and/or radiotherapy ever before
- •2\. Aged 18\-75
- •3\. There are at least two cycles of chemotherapy planned during the study program
- •4\. Eastern Cooperative Oncology Group (ECOG) performance status 0\-2
- •5\. Traditional Chinese Medicine (TCM) syndrome is differentiated as deficiency of spleen qi and stomach qi
- •6\. Anticipated survival time is more than 6 months
- •7\. All patients provided written informed consent before enrollment
Exclusion Criteria
- •1\. Complicated with other serious heart, liver, kidney, immune and hematopoietic system diseases
- •2\. Pregnant women or women who are breastfeeding
- •3\. Patients who were on active treatment for anaemia (i.e., EPO or blood transfusions)
- •4\. Patients who were receiving steroids to alleviate fatigue
- •5\. Patients who had been diagnosed with depression, anxiety disorders, mental illness and cognitive disorders
- •6\. Patients who had low platelet count or suffered from a bleeding disorder (e.g., haemophilia)
- •7\. Complicated with sepsis or bacteremia
- •8\. Patients who had lymphoedema at the area of the acupuncture points
- •9\. Patients who are allergic to stainless steel needle or had needle phobia
Outcomes
Primary Outcomes
Not specified
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