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Clinical Trials/EUCTR2015-002381-23-FR
EUCTR2015-002381-23-FR
Active, not recruiting
Phase 1

Comparison of the efficacy of IV paracetamol and IV ketoprofen in the treatment of renal colic in emergency department : a two-center double blind randomized study. - PIVKIV

CHU de Nîmes0 sitesSeptember 11, 2015

Overview

Phase
Phase 1
Intervention
Not specified
Conditions
Comparison of the efficacy of IV paracetamol and IV ketoprofen in the treatment of renal colic
Sponsor
CHU de Nîmes
Status
Active, not recruiting
Last Updated
9 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
September 11, 2015
End Date
TBD
Last Updated
9 years ago
Study Type
Interventional clinical trial of medicinal product
Sex
All

Investigators

Sponsor
CHU de Nîmes

Eligibility Criteria

Inclusion Criteria

  • informed consent
  • The patient is available for telephone follow\-up to one week
  • The patient is at least 18 years old.
  • suspected renal colic
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1\.2 Adults (18\-64 years) yes
  • F.1\.2\.1 Number of subjects for this age range 338
  • F.1\.3 Elderly (\>\=65 years) yes
  • F.1\.3\.1 Number of subjects for this age range 338

Exclusion Criteria

  • The patient has contreindication for a necessary treatment in this study.
  • The patient has an allergy to ketoprofen or paracetamol , of gastric or intestinal ulcer , bleeding disorders, a history of asthma triggered by taking ketoprofen or similar activity substances
  • The patient has hyperthermia, hemodynamic instability, oligoanuria .
  • The patient has an initial pain assessed by NRS 10/10 .
  • The patient has a history of aneurysm or aortic dissection, kidney transplant , single kidney, liver or kidney failure .
  • ketoprofen or paracetamol administration four hours before treatment to emergencies.aracétamol 4 heures avant le traitement en structure d'urgence.

Outcomes

Primary Outcomes

Not specified

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