Yata 2001.
Methods | Single‐centre parallel randomised controlled trial. Sample size: not reported Setting: 1 hospital in Inagawa Town (Japan) |
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Participants | 82 patients: 22 male, 60 female; mean age: PEG 75.1 (50 to 96), NGT 76.5 (38 to 93) Inclusion criteria: dysphagic patients Exclusion criteria: not reported |
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Interventions | PEG n = 42 NGT n = 40 |
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Outcomes |
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Notes | Study available only as a meeting abstract | |
Risk of bias | ||
Bias | Authors' judgement | Support for judgement |
Random sequence generation (selection bias) | Unclear risk | Not reported |
Allocation concealment (selection bias) | Unclear risk | Not reported |
Blinding of participants and personnel (performance bias) All outcomes | High risk | Not possible for this type of intervention |
Blinding of outcome assessment (detection bias) All outcomes | Unclear risk | Not explicitly described by the study investigators |
Incomplete outcome data (attrition bias) All outcomes | Unclear risk | Flow of patients was not clearly reported |
Selective reporting (reporting bias) | Low risk | Relevant outcomes were analysed, Outcome 7. was reported only for NGT group Outcomes 8 and 9 were reported only for the PEG group |
Other bias | High risk | Unpublished study |
GER: gastroesophogeal reflux ITT: intention‐to‐treat IV: intravenous NGT: nasogastric tube PEG: percutaneous endoscopic gastrostomy QoL: quality of life