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Clinical Trials/EUCTR2005-001622-91-GB
EUCTR2005-001622-91-GB
Active, not recruiting
Not Applicable

A randomised assessor blinded study to examine the role of skin testing in the prediction of peri-operative anaphylaxis and its correlation with mast cell tryptase and total IgE. - Peri-operative screening for sensitization to NMDAs

Royal Group Hospitals0 sites160 target enrollmentMay 9, 2005

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Prevalance of sensitivity of immune system to the four named neuromuscular blocking drugs in patients undergoing anaesthesia.
Sponsor
Royal Group Hospitals
Enrollment
160
Status
Active, not recruiting
Last Updated
14 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
May 9, 2005
End Date
TBD
Last Updated
14 years ago
Study Type
Interventional clinical trial of medicinal product
Sex
All

Investigators

Sponsor
Royal Group Hospitals

Eligibility Criteria

Inclusion Criteria

  • i) ASA class I\-II
  • ii) Scheduled for elective surgery that involves anaesthesia and the use of neuromuscular blocking drugs and expected to last at least 1 hour.
  • iii) Scheduled for elective surgery with no anticipated large blood loss or fluid shifts
  • iv) Planned post\-operative in patient stay to last at least four days.
  • 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) yes
  • F.1\.3\.1 Number of subjects for this age range

Exclusion Criteria

  • i) No previous history of anaphylaxis.
  • ii) No previous reaction to any of the medications used.
  • iii) Pregnancy.
  • iv) Acute exacerbation of any pre\-existing disease.
  • v) Not on any steroid or anti\-histamine medication at time of testing.

Outcomes

Primary Outcomes

Not specified

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