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Efficacy and Satisfaction With Remifentanil Analgesia in Parturients During the Childbirth

NCT02447757 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 66

Last updated 2016-07-26

No results posted yet for this study

Summary

Retrospective observational study to determine the efficacy of remifentanil during the delivery. Authors will search the data in period between 2010 and 2014 in cohort of 100 parturients and obtain data of analgesic efficacy (VAS score after remifentanil analgesia induction) and parturients satisfaction with the method.

Conditions

  • Complication of Labor and/or Delivery

Interventions

DRUG

remifentanil

Remifentanil analgesia during delivery

Sponsors & Collaborators

  • Hospital Sokolov

    collaborator UNKNOWN

  • Brno University Hospital

    lead OTHER

Eligibility

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

Timeline & Regulatory

Start
2010-01-31
Primary Completion
2015-01-31
Completion
2016-02-29

Countries

  • Czechia

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 NCT02447757 on ClinicalTrials.gov