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Analgesia in the Second Stage of Labour

NCT04391075 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 1007

Last updated 2020-05-19

No results posted yet for this study

Summary

This study investigates efficacy, safety and childbirth experience in women receiving pudendal block during the final stage of delivery. It is an observational study and half of included primarous women recieve a pudendal block.

Conditions

  • Childbirth Experience
  • Urinary Retention
  • Satisfaction, Personal
  • Pain, Obstetric

Interventions

PROCEDURE

Pudendal nerve block

Pudendal nerve block provided during last fase of delivery

Sponsors & Collaborators

  • Oslo University Hospital

    lead OTHER

Principal Investigators

  • Anne Flem Jacobsen, PhD · Univeristy of Oslo

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2017-01-01
Primary Completion
2019-05-01
Completion
2019-05-31

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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 NCT04391075 on ClinicalTrials.gov