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.
Investigators
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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