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Clinical Trials/NCT06357468
NCT06357468CompletedNot Applicable

Analysis of Pain Management and Pain Perception Intrapartum and Postpartum in Women with Vaginal Births in Difference Between Physician-led and Midwife-led Birth

Martin-Luther-Universität Halle-Wittenberg1 site in 1 country237 target enrollmentStarted: January 1, 2023Last updated:
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Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
237
Locations
1
Primary Endpoint
Pain perception
Study OverviewStudy DesignEligibility CriteriaOutcomesInvestigatorsSitesRecords & IdentifiersSimilar Trials

Study Overview

Brief Summary

The aim of the analysis is to describe the differences and similarities in obstetric pain management and pain perception intrapartum and postpartum in women with vaginal births in contrast to physician-led births and midwife-led births

Study Design

Study Type
Observational
Observational Model
Cohort
Time Perspective
Retrospective

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
Female
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •Understanding written and spoken German
  • •Declaration of consent

Exclusion Criteria

  • •under 18 years
  • •incomplete answered questionaire

Outcomes

Primary Outcomes

Pain perception

Time Frame: intrapartum (start of labour until end of labour) and postpartum first 3 days after birth

Measured by visual pain scale (1-10)

Secondary Outcomes

  • Satisfaction with pain therapy(intrapartum (start of labour until end of labour) and postpartum first 3 days after birth)
  • Pain perception in women with perineal tear grade III(postpartum first 3 days after birth)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Marcus Riemer, MD

Principal Investigator

Martin-Luther-Universität Halle-Wittenberg

Study Sites (1)

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