CompletedNot Applicable

Establishment and Evaluation of a Post Caesarean Acute Pain Service (PCAPS)

Czechia407 participantsStarted 2009-10

Plain-language 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.

Who can participate

SexFEMALE

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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

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.

What they're measuring

Visual Analogue Scale (VAS)

Timeframe: 72 hours after Caesarean Section (CS)

Trial details

NCT IDNCT02062320

SponsorBrno University Hospital

Sponsor typeOTHER

Study typeOBSERVATIONAL

Primary completion2011-10

View on ClinicalTrials.gov More The Efficacy of Analgesic Methods After Caesarean Section trials