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.
Investigators
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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