- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00736060
Clinical and Laboratory Characteristics of Sickle Cell Anemia Patients Admitted With Fever
Study the Clinical and Laboratory Characteristics and the Outcome of Sickle Cell Anemia Patients Admitted to the Pediatric Ward Because of Fever as the Presenting Symptom
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
The actual protocol for SCA patients admitted with fever is to obtain blood cultures and start empiric antibiotic treatment.
The study cohort included 60 SCA patients actually treated in the Pediatric Hematology Unit.
Study Type
Enrollment (Anticipated)
Contacts and Locations
Study Locations
-
-
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Afula, Israel, 18101
- Pediatric Hematology Unit - Ha'Emek Medical Center
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-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria: All patients admitted with fever as the only presenting symptom.
Exclusion Criteria: Patients admitted with another causes related or unrelated to sickle cell disease and have also fever.
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
1
Sickle cell anemia
|
Summary of clinical and laboratory data
|
2
Sickle cell thalassemia
|
Summary of clinical and laboratory data
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Carina Levin, MD, Pediatric Hematology Unit - Ha'Emek Medical Center - Afula - 18101 - Israel
- Principal Investigator: Ilena Arshinov, MD, Pediatric Dpt B - Ha'Emek Medical Center - Afula - Israel
Study record dates
Study Major Dates
Study Start
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 0027-08-EMC
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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