| Study characteristics |
Eligibility criteria (Insert eligibility criteria for each characteristic as defined in the protocol) |
Yes | No | Unclear |
Location in text (pg & ¶/fig/table) |
|
| Type of study | Randomised controlled trial | |||||
| Controlled clinical trial (quasi‐randomised trial) |
||||||
| Participants | Healthy parturients requesting for epidural analgesia during labour | |||||
| Types of intervention | Automated mandatory bolus Basal infusion |
|||||
| Types of outcome measures | 1. Risk of breakthrough pain with need for anaesthetic intervention (dichotomous) 2. Risk of caesarean delivery (dichotomous) 3. Risk of instrumental delivery (dichotomous) 4. Duration of labour (continuous) 5. Total dose of local anaesthetic per hour (continuous) 6. Maternal satisfaction (continuous) 7. Apgar scores (continuous) |
|||||
| INCLUDE | EXCLUDE | |||||
| Reason for exclusion | ||||||
| Notes: | ||||||
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