Programmed Intermittent Epidural Bolus For Laboring Obstetrical Women (NCT03712735) | Clinical Trial Compass
CompletedPhase 4
Programmed Intermittent Epidural Bolus For Laboring Obstetrical Women
Canada390 participantsStarted 2018-10-23
Plain-language summary
Comparison of three programmed intermittent epidural bolus (PIEB) pump settings for maintenance of labour analgesia.
Who can participate
Age range19 Years
SexFEMALE
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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* Singleton, vertex presentations at term (37-42 weeks gestational age)
* \</= 5cm cervical dilation at the time of epidural anesthesia request
* ASA 2-3 patients aged 19 or over who are able to provide informed consent
Exclusion Criteria:
* Contraindications to neuraxial analgesia or risk factors likely to affect placement or function of the epidural
* History of hypersensitivity or idiosyncratic reaction to local anesthetics or opioids
* Current or historical evidence of any significant medical conditions
* Clinical settings in which continuous epidural infusion may be preferable
* Risk factors significantly increasing the need for Cesarean delivery
* Anticipated fetal abnormalities