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Clinical Trials/NCT02447757
NCT02447757
Completed
Not Applicable

Efficacy and Satisfaction With Remifentanil Analgesia in Parturients During the Childbirth: Retrospective Observational Study

Brno University Hospital2 sites in 1 country66 target enrollmentJanuary 2010

Overview

Phase
Not Applicable
Intervention
remifentanil
Conditions
Complication of Labor and/or Delivery
Sponsor
Brno University Hospital
Enrollment
66
Locations
2
Primary Endpoint
Efficacy of remifentanyl analgesia during the delivery
Status
Completed
Last Updated
9 years ago

Overview

Brief 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.

Detailed Description

In retrospective observational study will authors search the documentation of parturients. The cohort size is estimated to 100 subjects, in period between 2010-2014. Excluded will be all patients who did not signed the informed consent for processing with their medical data.The main aim is to evaluate the efficacy of the remifentanil analgesia in parturients in the first phase of delivery. The analgesic efficacy will be evaluated by the change in VAS (visual analogue scale) score after induction of remifentanil analgesia Satisfaction will be evaluated by the questionary.

Registry
clinicaltrials.gov
Start Date
January 2010
End Date
February 2016
Last Updated
9 years ago
Study Type
Observational
Sex
Female

Investigators

Sponsor
Brno University Hospital
Responsible Party
Principal Investigator
Principal Investigator

Petr Štourač, MD

MD, Ph.D

Brno University Hospital

Eligibility Criteria

Inclusion Criteria

  • parturients during the delivery
  • administered remifentanil analgesia
  • signed informed consent

Exclusion Criteria

  • informed consent not signed
  • missing data about the analgetic method a analgetic efficacy

Arms & Interventions

Parturients with remifentanil analgesia

Parturients after induction of remifentanyl analgesia during the delivery

Intervention: remifentanil

Outcomes

Primary Outcomes

Efficacy of remifentanyl analgesia during the delivery

Time Frame: VAS score before the induction of remifentanyl infusion and 1hour after initiation of remifentanil analgesia during the first phase of delivery

To evaluate the efficacy of remifentanil analgesia during the first phase of delivery in parturients by observing changes in VAS score

Secondary Outcomes

  • Patient satisfaction with analgetic method(Before initiation of anagetic method (first phase of delivery) and 1hour after childbirth)

Study Sites (2)

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