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Parturient Satisfaction With Epidural Analgesia by PCEA or Manual Boluses

NCT06094946 · Status: NOT_YET_RECRUITING · Type: OBSERVATIONAL · Enrollment: 100

Last updated 2024-04-24

No results posted yet for this study

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.

Conditions

  • Labor Pain

Interventions

DRUG

Ropivacaine Hydrocloride

1 mg/ml

DRUG

Fentanyl Citrate

2.5 micrograms/ml

Sponsors & Collaborators

  • Helsinki University Central Hospital

    collaborator OTHER

  • Women's Hospital HUS

    lead OTHER

Principal Investigators

  • Riina Jernman, MD PhD · Helsinki University Hospital Women's hospital

Eligibility

Min Age
18 Years
Max Age
55 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2024-12-31
Primary Completion
2025-02-28
Completion
2025-02-28

Countries

  • Finland

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06094946 on ClinicalTrials.gov