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| Methods | Prospective, randomized, double‐blind study |
| Participants | A total of 60 nulliparous women |
| Interventions | Participants were randomized to receive an epidural infusion of either 0.125% plain bupivacaine or 0.0625% bupivacaine with 2.5µg/ml fentanyl |
| Outcomes | The primary outcome was pain and motor block. Secondary outcomes were maternal side effects and cardio‐tocograph abnormalities |
| Notes | — |
