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Penicillin Allergy in Shfayim Clinic

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
 
ClinicalTrials.gov Identifier: NCT03499457
Recruitment Status : Unknown
Verified April 2018 by Dr. Lital Goldberg, Clalit Health Services.
Recruitment status was:  Not yet recruiting
First Posted : April 17, 2018
Last Update Posted : April 17, 2018
Sponsor:
Information provided by (Responsible Party):
Dr. Lital Goldberg, Clalit Health Services

Brief 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.

Condition or disease Intervention/treatment Phase
Penicillin Allergy Drug: Amoxicillin Not Applicable

Detailed 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.

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Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 100 participants
Intervention Model: Single Group Assignment
Masking: None (Open Label)
Primary Purpose: Other
Official Title: Penicillin Allergy in Shfayim Clinic
Estimated Study Start Date : June 2018
Estimated Primary Completion Date : January 2019
Estimated Study Completion Date : June 2019

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Allergy

Arm Intervention/treatment
Experimental: treatment
penicillin chalange test, as descibed.
Drug: Amoxicillin
chalange test of 50 mg, and after an hour 500 mg




Primary Outcome Measures :
  1. immidiate urticarial reaction [ Time Frame: with 2 hours of test ]
    shortness of breath, angioedema


Secondary Outcome Measures :
  1. rash [ Time Frame: with 2 hours of test ]
    body rash or itch seen by patient or physician



Information from the National Library of Medicine

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Ages Eligible for Study:   5 Years to 80 Years   (Child, Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

penicillin allergy in the medical record

Exclusion Criteria:

pregnancy lack of informed consent


Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03499457


Contacts
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Contact: lital f goldberg, MD. MPH. 972544248284 litalmargalith@gmail.com

Sponsors and Collaborators
Clalit Health Services
Investigators
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Principal Investigator: lital f goldberg, MD. MPH Clalit Health Services

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Responsible Party: Dr. Lital Goldberg, dr lital goldberg, Clalit Health Services
ClinicalTrials.gov Identifier: NCT03499457    
Other Study ID Numbers: 0185-17-COM2
First Posted: April 17, 2018    Key Record Dates
Last Update Posted: April 17, 2018
Last Verified: April 2018

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Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No
Keywords provided by Dr. Lital Goldberg, Clalit Health Services:
Penicillin Allergy
chalenge test
primary clinic
Additional relevant MeSH terms:
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Hypersensitivity
Drug Hypersensitivity
Immune System Diseases
Drug-Related Side Effects and Adverse Reactions
Chemically-Induced Disorders
Amoxicillin
Penicillins
Anti-Bacterial Agents
Anti-Infective Agents