Safety of Ibuprofen After Major Orthopaedic Surgeries

Last updated: April 26, 2023
Sponsor: Naestved Hospital
Overall Status: Active - Recruiting

Phase

4

Condition

Acute Pain

Pain

Chronic Pain

Treatment

N/A

Clinical Study ID

NCT05575700
001CCWL2022
  • Ages > 18
  • All Genders

Study Summary

Safety of an eight-day treatment with ibuprofen after primary hip and knee arthroplasties.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • Patients scheduled for elective primary hip and knee arthroplasty.
  • Age ≥ 18 years.
  • Planned postoperative treatment with NSAID.
  • Negative pregnancy test for women in the fertile age.
  • Informed consent.

Exclusion

Exclusion Criteria:

  • Unable to understand or speak Danish.
  • Allergy to or contraindications against ibuprofen.

Study Design

Total Participants: 2904
Study Start date:
April 17, 2023
Estimated Completion Date:
December 31, 2026

Study Description

Hip and knee arthroplasty surgeries are some of the most frequently performed planned procedures in the western world. Multimodal analgesic treatment is the leading analgesic treatment principle, with NSAIDs as an essential part. Ibuprofen, the most frequently prescribed NSAID, is effective in reducing acute postoperative pain. However, ibuprofen may be associated with various serious adverse events, including death, cardiovascular morbidity, gastrointestinal ulcer, and renal impairment. The balance between beneficial and harmful effects of a short-term postoperative treatment with ibuprofen after elective hip and knee arthroplasty is unknown.

Objectives: to assess the adverse events of an eight-day treatment of postoperative pain with ibuprofen in patients undergoing elective primary hip or knee arthroplasty.

Intervention: the participants will be randomized in two groups: a) oral ibuprofen 400 mg 3 times daily for eight days. b) identical oral placebo 3 times daily for eight days.

Design and trial size: PERISAFE is a randomized, placebo-controlled multicentre trial with centralized computer-generated allocation sequence and allocation concealment with unknown block size. Patients, investigators, assessors, caregivers, data-managers, writers of the manuscript, and statisticians will be blinded. A total of 2904 eligible patients are needed to detect or discard an effect corresponding to a relative risk reduction of 1/3 with an acceptable risk of type I error of 5 % and of type II error of 20 %, and a proportion of the composite outcome of serious adverse events of 8% in the experimental group.

Sub-studies:

  • One-year follow-up on the composite primary outcome.

  • Subgroup analysis on predictors of chronic pain and opioid consumption at 90-days, and one-year after surgery.

  • Coherence of preoperative use of diuretics, ACE-inhibitors or Angiotensin-II-antagonists and postoperative risk of renal failure.

Connect with a study center

  • Private Hospital Gildhøj

    Brøndby, 2605
    Denmark

    Site Not Available

  • Bispebjerg Hospital

    Copenhagen NV, 2400
    Denmark

    Site Not Available

  • Aalborg University Hospital

    Farsø, 9640
    Denmark

    Site Not Available

  • Aalborg University Hospital

    Frederikshavn, 9900
    Denmark

    Site Not Available

  • Gentofte Hospital

    Hellerup, 2900
    Denmark

    Active - Recruiting

  • Nordsjællands Hospital Hillerød

    Hillerød, 3400
    Denmark

    Site Not Available

  • Zealand University Hospital

    Køge, 4600
    Denmark

    Site Not Available

  • Næstved Hospital

    Næstved, 4700
    Denmark

    Active - Recruiting

  • Odense University Hospital

    Odense, 3900
    Denmark

    Site Not Available

  • Silkeborg Regional Hospital

    Silkeborg, 8600
    Denmark

    Site Not Available

  • Svendborg Hospital

    Svendborg, 5700
    Denmark

    Site Not Available

  • Vejle Sygehus

    Vejle, 7100
    Denmark

    Site Not Available

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