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NCT03499457 Clinical Trial

Penicillin Allergy in Shfayim Clinic

Penicillin Allergy Clinical Trial

Official title:
Penicillin Allergy in Shfayim Clinic

Clinical Trial Details — Status: Not yet recruiting

Administrative data
NCT number NCT03499457
Other study ID # 0185-17-COM2
Secondary ID
Status Not yet recruiting
Phase N/A
First received April 8, 2018
Last updated April 8, 2018
Start date June 2018
Est. completion date June 2019

Study information
Verified date April 2018
Source Clalit Health Services
Contact lital f goldberg, MD. MPH.
Phone 972544248284
Email litalmargalith@gmail.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

revising penicillin allergy in the medical records, by taking full medical history and giving a challange test, in order to imrove the medical records and treatment possibilities.

Description:

issuing a list of patients with a title of penicillin allergy in their medical record. inviting these patients to an appointmnet with their family physician, in which a specific history will be take to evaluate the quality of the allergy.

patients with suscpition of a life threatening allergic reaction will be reffered to an allergy clinic for the challange test. the rest of the pateints will be given the test in the primary clinic: 1ml (50 grams) of amoxicillin, and an hour later a full dose of 500 mg amoxicillin.

after determining no allergic reaction develops the title will be erased from the medical record.

Recruitment information / eligibility
Status Not yet recruiting
Enrollment 100
Est. completion date June 2019
Est. primary completion date January 2019
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 5 Years to 80 Years
Eligibility Inclusion Criteria:

penicillin allergy in the medical record

Exclusion Criteria:

pregnancy lack of informed consent

Study Design

Related Conditions & MeSH terms

Intervention

Drug:
• Amoxicillin
chalange test of 50 mg, and after an hour 500 mg

Locations
Country Name City State
n/a

Sponsors (1)
Lead Sponsor Collaborator
Clalit Health Services

Outcome
Type Measure Description Time frame Safety issue
Primary immidiate urticarial reaction shortness of breath, angioedema with 2 hours of test
Secondary rash body rash or itch seen by patient or physician with 2 hours of test
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