Ueyama 1992.
Study characteristics | ||
Methods | RCT | |
Participants | 100 women (60 non‐labouring women scheduled for elective caesarean and 40 labouring women for emergency caesarean) Exclusion criteria: women with placenta praevia, abruptio placenta; toxaemia |
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Interventions |
Ephedrine (various doses) versus control Group1: ephedrine 5 mg Group 2: ephedrine 10 mg Group 3: no ephedrine Ephedrine was administered with the spinal. All women received a standardised preload of 1000 mL Ringer's lactate, a standardised spinal anaesthetic technique and dose. |
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Outcomes | Maternal: hypotension; SAP | |
Notes | Hypotension was defined as SAP lower than 80 mmHg | |
Risk of bias | ||
Bias | Authors' judgement | Support for judgement |
Random sequence generation (selection bias) | Unclear risk | Methods not described |
Allocation concealment (selection bias) | Unclear risk | Methods not describe |
Blinding of participants and personnel (performance bias) All outcomes | Unclear risk | Blinding not stated |
Blinding of outcome assessment (detection bias) All outcomes | Unclear risk | Blinding not stated |
Incomplete outcome data (attrition bias) All outcomes | Unclear risk | Losses to follow‐up: not stated |
Selective reporting (reporting bias) | Unclear risk | Unclear reporting |
Other bias | Unclear risk | Unclear reporting |