Paracetamol, ibuprofen and dexamethasone for pain treatment after total hip arthroplasty: protocol for the randomised, placebo-controlled, parallel 4-group, blinded, multicentre RECIPE trial.
Acetaminophen
/ therapeutic use
Analgesics
/ therapeutic use
Analgesics, Opioid
/ therapeutic use
Anti-Inflammatory Agents, Non-Steroidal
Arthroplasty, Replacement, Hip
/ adverse effects
Dexamethasone
/ therapeutic use
Double-Blind Method
Glucocorticoids
/ therapeutic use
Humans
Ibuprofen
Morphine
Multicenter Studies as Topic
Pain, Postoperative
/ drug therapy
Randomized Controlled Trials as Topic
Adult anaesthesia
Anaesthesia in orthopaedics
Clinical trials
Hip
PAIN MANAGEMENT
Pain management
Journal
BMJ open
ISSN: 2044-6055
Titre abrégé: BMJ Open
Pays: England
ID NLM: 101552874
Informations de publication
Date de publication:
01 09 2022
01 09 2022
Historique:
entrez:
3
10
2022
pubmed:
4
10
2022
medline:
6
10
2022
Statut:
epublish
Résumé
Multimodal analgesia with paracetamol, non-steroidal anti-inflammatory drug and glucocorticoid is recommended for hip arthroplasty, but with uncertain effects of the different combinations. We aim to investigate benefit and harm of different combinations of paracetamol, ibuprofen and dexamethasone following total hip arthroplasty. RECIPE is a randomised, placebo-controlled, parallel 4-group, blinded trial with 90-day and 1-year follow-up performed at nine Danish hospitals. Interventions are initiated preoperatively and continued for 24 hours postoperatively. Eligible participants undergoing total hip arthroplasty are randomised to:group A: oral paracetamol 1000 mg × 4+oral ibuprofen 400 mg × 4+intravenous placebo; group B: oral paracetamol 1000 mg × 4+intravenous dexamethasone 24 mg+oral placebo; group C: oral ibuprofen 400 mg × 4+intravenous dexamethasone 24 mg+oral placebo; group D: oral paracetamol 1000 mg × 4+oral ibuprofen 400 mg × 4+intravenous dexamethasone 24 mg.Primary outcome is cumulative opioid consumption at 0-24 hours. Secondary outcomes are pain at rest, during mobilisation and during a 5 m walk and adverse events. Follow-up includes serious adverse events and patient reported outcome measures at 90 days and 1 year. A total of 1060 participants are needed to demonstrate a difference of 8 mg in 24-hour morphine consumption assuming an SD of 24.5 mg, a risk of type I errors of 0.0083 and a risk of type 2 errors of 0.2. Primary analysis will be a modified intention-to-treat analysis.With this trial we aim to verify recommendations for pain treatment after total hip arthroplasty, and investigate the role of dexamethasone as an analgesic adjuvant to paracetamol and ibuprofen. This trial is approved by the Region Zealand Committee on Health Research Ethics (SJ-799). Plans for dissemination include publication in peer-reviewed journals and presentation at scientific meetings. NCT04123873.
Identifiants
pubmed: 36190737
pii: bmjopen-2021-058965
doi: 10.1136/bmjopen-2021-058965
pmc: PMC9438203
doi:
Substances chimiques
Analgesics
0
Analgesics, Opioid
0
Anti-Inflammatory Agents, Non-Steroidal
0
Glucocorticoids
0
Acetaminophen
362O9ITL9D
Morphine
76I7G6D29C
Dexamethasone
7S5I7G3JQL
Ibuprofen
WK2XYI10QM
Banques de données
ClinicalTrials.gov
['NCT04123873']
Types de publication
Clinical Trial Protocol
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
e058965Informations de copyright
© Author(s) (or their employer(s)) 2022. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.
Déclaration de conflit d'intérêts
Competing interests: None declared.
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