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. 2018 Oct 30;2018(10):CD000323. doi: 10.1002/14651858.CD000323.pub3

Chan 2012.

Methods Randomisation by random sequences on black paper
Single‐blind (participants blinded): outcome assessors blinded
Participants 1 centre in Hong Kong
87 participants with neurogenic dysphagia with similar baseline characteristics
60 (69%) participants with dysphagia due to cerebral infarct < 6 months; other causes of neurogenic dysphagia include intracranial haemorrhage, vascular dementia, Parkinson's disease
Clinical evidence of dysphagia
Interventions All groups given routine swallowing therapy
Rx 1: true acupuncture (n = 20)
 Rx 2: sham acupuncture that did not puncture true acupoints lying on a meridian (n = 19)
 C: routine swallowing therapy only (n = 48)
 Treatment for up to 4 weeks
Outcomes Outcomes: Royal Brisbane Hospital Outcome Measure Scale (RBHOMS), swallow function by consistencies of ingested food and fluid
Notes Exclusions: structural oral, pharyngeal, or oesophageal disease; severe primary disease of the liver, kidneys, hematopoietic system, or endocrine system; malignant tumour or infectious disease; inability to follow commands
 Follow‐up: 3 months
Risk of bias
Bias Authors' judgement Support for judgement
Random sequence generation (selection bias) Low risk Randomisation by random sequences
Allocation concealment (selection bias) Low risk Allocation concealed in opaque envelopes
Blinding (performance bias and detection bias) 
 All outcomes Low risk Single (participants) blinded
Blinding of participants and personnel (performance bias) 
 All outcomes Low risk Single (participants) blinded
Blinding of outcome assessment (detection bias) 
 All outcomes Low risk Outcome assessors blinded
Incomplete outcome data (attrition bias) 
 All outcomes Low risk No losses to follow‐up reported
Selective reporting (reporting bias) Low risk All outcomes reported
Other bias Low risk None identified