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Clinical Trials/NCT02062320
NCT02062320
Completed
Not Applicable

Establishment and Evaluation of a Post Caesarean Acute Pain Service

Brno University Hospital1 site in 1 country407 target enrollmentOctober 2009
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ConditionsThe Efficacy of Analgesic Methods After Caesarean Section

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
The Efficacy of Analgesic Methods After Caesarean Section
Sponsor
Brno University Hospital
Enrollment
407
Locations
1
Primary Endpoint
Visual Analogue Scale (VAS)
Status
Completed
Last Updated
12 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSitesSimilar Trials

Overview

Brief Summary

The aim of this study is to compare the efficacy of analgesic methods after Caesarean Section before and after Post Caesarean Acute Pain Service establishing.

Registry
clinicaltrials.gov
Start Date
October 2009
End Date
October 2011
Last Updated
12 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

  • •Caesarean Section performed from October 2009 to October 2011 (study period)
  • •completed "Evaluation of postoperative analgesia after Caesarean Section" form.

Exclusion Criteria

  • •Not completed "Standard Evaluation of postoperative analgesia after Caesarean Section" form.

Outcomes

Primary Outcomes

Visual Analogue Scale (VAS)

Time Frame: 72 hours after Caesarean Section (CS)

Comparison of pain intensity (Visual Analogue Scale (VAS)) during the postoperative period (72 hours) between the two groups according to postoperative analgesic method and method of anaesthesia.

Secondary Outcomes

  • VAS score above 4(72 hours after CS)
  • Additional Analgesic Requests (AAR) Count(72 hours after CS)
  • Analgesia related complication Rate(72 hours after CS)

Study Sites (1)

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