CompletedPhase 3

Traumatologic Acute Pain Management With Fentanyl Transdermal Therapeutic System (TTS)

Austria145 participantsStarted 2019-06-30

Plain-language summary

Aim of the study is an examination whether a modified perioperative pain management system, that integrates the 2017 European Society of Anaesthesiology (ESA) guidelines for treatment of postoperative Delirium, can improve patient's wellbeing in comparison to the current certified standard management.

Who can participate

Age range18 Years

SexALL

See this in plain English?

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

Inclusion Criteria: * adult patients with hip fractures that have to be operated (ICD S72.01-S72.2) Exclusion Criteria: * severe liver damage * ongoing dialysis therapy * Monoamine oxidase inhibitor intake * inability to give consent to trial participation

What they're measuring

Patient's wellbeing in the awakening room

Timeframe: 1 year

Trial details

NCT IDNCT04026022

SponsorMedical University of Graz

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2020-03-06

View on ClinicalTrials.gov More Hip Fractures (ICD-10 72.01-72.2) trials