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Clinical Trials/CTIS2024-513688-25-01
CTIS2024-513688-25-01
Active, not recruiting
Phase 1

A blinded randomized study investigating the effect of pericapsular nerve group (PENG) block on postoperative pain after peri-acetabular osteotomy

Rigshospitalet0 sites90 target enrollmentApril 30, 2024
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Conditionsperiacetabular osteotomyTherapeutic area: Analytical, Diagnostic and Therapeutic Techniques and Equipment [E] - Anesthesia and Analgesia [E03]

Overview

Phase
Phase 1
Intervention
Not specified
Conditions
periacetabular osteotomy
Sponsor
Rigshospitalet
Enrollment
90
Status
Active, not recruiting
Last Updated
last year
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
April 30, 2024
End Date
TBD
Last Updated
last year
Study Type
Interventional clinical trial of medicinal product
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • •Patients \= 18 years old, Informed consent, Scheduled for periacetabular osteotomy under general anesthesia with intubation, American Society of Anesthesiologists (ASA) physical status classification I to III, Can read and understand Danish

Exclusion Criteria

  • •Known allergy to ropivacaine, Daily use of opioids, gabapentin or tricyclic antidepressant (regardless of dose) within the last four weeks prior to surgery, Contraindications to Celocoxib, NSAIDs or paracetamol

Outcomes

Primary Outcomes

Not specified

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