Williams 2003.
Methods | Randomised crossover study | |
Participants | Stable heart failure Age range 38 to 75 years Mostly male (N = 15) |
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Interventions | Diamorphine 1 or 2 mg given intravenously Compared to intravenous saline |
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Outcomes | Primary outcome of breathlessness was not measured Oxygen consumption Exercise duration Respiratory rate |
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Notes | Naloxone 0.4 mg was given at the end of the test | |
Risk of bias | ||
Bias | Authors' judgement | Support for judgement |
Random sequence generation (selection bias) | Unclear risk | The study authors did not clearly state the methods of random sequence generation. |
Allocation concealment (selection bias) | Unclear risk | The study authors did not clearly state the methods of allocation concealment. |
Blinding of participants and personnel (performance bias) All outcomes | Unclear risk | The study authors did not clearly state whether they blinded participants and personnel. |
Blinding of outcome assessment (detection bias) All outcomes | Unclear risk | The study authors did not clearly state whether or not they performed blinding of outcome assessment. |
Incomplete outcome data (attrition bias) All outcomes | Low risk | The study authors reported all follow‐up and completion data. |
Selective reporting (reporting bias) | Low risk | We did not detect any selective reporting bias. |
Other bias | Low risk | We judged that this trial appeared to be free of other sources of bias. |
Size bias | High risk | This study had a small sample size; there were < 50 participants per treatment arm. |