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Clinical Trials/EUCTR2008-008475-34-AT
EUCTR2008-008475-34-AT
Active, not recruiting
Not Applicable

The effect of remifentanil on the reversal of established sunburn-induced hyperalgesia in human volunteers.

Abteilung für Anaesthesie und Intensivmedizin, Medizinische Universität Wien0 sitesJanuary 27, 2009

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
This is a volunteer study in healthy volunteers. Pain research, reversal of hyperalgesia by IMP is studied
Sponsor
Abteilung für Anaesthesie und Intensivmedizin, Medizinische Universität Wien
Status
Active, not recruiting
Last Updated
14 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
January 27, 2009
End Date
TBD
Last Updated
14 years ago
Study Type
Interventional clinical trial of medicinal product
Sex
All

Investigators

Sponsor
Abteilung für Anaesthesie und Intensivmedizin, Medizinische Universität Wien

Eligibility Criteria

Inclusion Criteria

  • Men or women, aged between 19 and 40 years
  • Body mass index between 15th and 85th percentile
  • Normal findings in the medical history and physical examination
  • Drug free for 1 week prior to the study day
  • 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
  • F.1\.3 Elderly (\>\=65 years) no
  • F.1\.3\.1 Number of subjects for this age range

Exclusion Criteria

  • Any of the following will exclude a subject from the study:
  • Regular use of medication especially analgesics
  • Abuse of alcoholic beverages, drug abuse
  • History of asthma
  • Participation in a clinical trial in the 2 weeks preceding the study
  • Symptoms of a clinically relevant illness in the 2 weeks before the first study day
  • Resting systolic blood pressure \>135 mmHg or diastolic blood pressure \>85 mmHg
  • Acute skin diseases like sunburn or skin lesions on the relevant areas and UV sensitive skin conditions, like Xeroderma pigmentosa
  • Pregnancy or breast feeding

Outcomes

Primary Outcomes

Not specified

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