UnknownNot Applicable

Parturient Satisfaction With Epidural Analgesia by PCEA or Manual Boluses

Finland100 participantsStarted 2024-12

Plain-language summary

Those prospective parturients that express that they may want an epidural labour analgesia for their delivery will be informed about the possibility to choose between a pump driven epidural or midwife administered intermittent boluses.

Who can participate

Age range18 Years – 55 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: * Age 18 years or older * Admitted to the delivery hospital with the prospect of vaginal delivery * On admission when questioned about planned analgesia expresses that may want an epidural analgesia for the planned vaginal delivery * After reading the study prochure signs the participation (consent) form * Sufficient command of Finnish or Swedish to facilitate interview Exclusion Criteria: * Contraindications for epidural analgesia * Planned cesarean delivery * Age under 18 years

What they're measuring

Parturient satisfaction with analgesia

Timeframe: During use of labour analgesia (up to 6 hours)

Trial details

NCT IDNCT06094946

SponsorWomen's Hospital HUS

Sponsor typeOTHER

Study typeOBSERVATIONAL

Primary completion2025-02

Contact for this trial

Antti J Vaananen, MD PhD

+358504271850 antti.vaananen@hus.fi

View on ClinicalTrials.gov More Labor Pain trials