Actively Recruiting

Phase 3
Age: 18Years - 85Years
All Genders
NCT06404177

Enantyum® IV Versus Piroxen® IM in Emergency Pain Management

Led by Riadh Boukef · Updated on 2024-05-08

300

Participants Needed

1

Research Sites

58 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

For pain of traumatic origin, the RICE protocol (Rest, Ice, Compression, Elevation) is the main therapeutic measure during the first 4 to 5 days post-trauma. However, there is currently insufficient evidence that this protocol is effective \[4\]. In the emergency department, paracetamol, NSAIDs or a combination of several molecules are generally prescribed. Patients even use these drugs without a prescription. The aim of this study is to Compare the effect of dexketoprofen® IV versus piroxen® IM in the treatment of pain in emergency departments.

CONDITIONS

Official Title

Enantyum® IV Versus Piroxen® IM in Emergency Pain Management

Who Can Participate

Age: 18Years - 85Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients over 18 years of age who require pain relief for acute traumatic injury pain
  • Patients able to provide written informed consent
Not Eligible

You will not qualify if you...

  • Patients unable or unwilling to give consent or communicate effectively
  • Patients with chronic pain conditions
  • Known allergy or adverse reaction to piroxicam or dexketoprofen trometamol
  • Pregnant women
  • Patients with liver cirrhosis

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Sahloul University Hospital

Sousse, Tunisia, 5000

Actively Recruiting

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Research Team

R

Riadh Boukef, professor

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

QUADRUPLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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