| Trial name or title | ANODE: Prophylactic antibiotics for the prevention of infection following operative delivery. |
| Methods | Participants are randomly allocated into two groups. |
| Participants | Healthy women aged 16 years and over who have had an operative vaginal delivery. |
| Interventions | Co‐amoxiclav versus placebo, A single intravenous dose (1 g amoxycillin/200 mg clavulanic acid in 20 mL water for injections for active drug, 20 mL 0.9% saline for placebo). |
| Outcomes | Confirmed or suspected maternal infection within 6 weeks of delivery. |
| Starting date | September 2009. |
| Contact information | Mrs Shan Gray. NPEU Clinical Trials Unit, Oxford (UK) |
| Notes | Expected to finish in August 2017. EudraCT number: 2015‐000872‐89. |
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