Mo 2016.
Methods | Design: parallel RCT Randomisation method: random number table Blinding: no Power calculation: no Dropouts/withdrawals: no |
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Participants | Cancer patients after chemotherapy with expected survival time of more than 6 months, Karnofsky ≥ 60, and WBC count less than 4 × 109/L; diagnosed with the Chinese medicine syndrome of qi and blood insufficiency Number (treatment/control): 82 (41/41) Mean age (range): 55.5 (34‐69) Gender (M/F): 48/34 Country: Guangdong province, China Setting: hospital |
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Interventions | Moxa stick vs conventional medicine Treatment group
Control group
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Outcomes | WBC count and Karnofsky score at the end of treatment | |
Notes | — | |
Risk of bias | ||
Bias | Authors' judgement | Support for judgement |
Random sequence generation (selection bias) | Low risk | Random number table |
Allocation concealment (selection bias) | Unclear risk | No relevant description |
Incomplete outcome data (attrition bias) All outcomes | Low risk | There was no loss to follow‐up. All participants were included in the analysis. |
Selective reporting (reporting bias) | Unclear risk | Limited outcome measures were reported. |
Other bias | Unclear risk | There was no statement about group similarity. |
Blinding of participants and personnel (performance bias) All outcomes | High risk | No blinding |
Blinding of outcome assessment (detection bias) Subjective outcomes | High risk | No blinding |
Blinding of outcome assessment (detection bias) Objective outcomes | Low risk | No blinding; however, machine‐measured objective outcomes were not influenced substantially |