Clinical and Laboratory Characteristics of Sickle Cell Anemia Patients Admitted With Fever
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ClinicalTrials.gov Identifier: NCT00736060 |
Recruitment Status :
Completed
First Posted : August 15, 2008
Last Update Posted : August 26, 2011
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Sponsor:
HaEmek Medical Center, Israel
Information provided by (Responsible Party):
Dr Koren Ariel, HaEmek Medical Center, Israel
Tracking Information | |||||||
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First Submitted Date | August 14, 2008 | ||||||
First Posted Date | August 15, 2008 | ||||||
Last Update Posted Date | August 26, 2011 | ||||||
Study Start Date | May 2008 | ||||||
Primary Completion Date | Not Provided | ||||||
Current Primary Outcome Measures | Not Provided | ||||||
Original Primary Outcome Measures | Not Provided | ||||||
Change History | |||||||
Current Secondary Outcome Measures | Not Provided | ||||||
Original Secondary Outcome Measures | Not Provided | ||||||
Current Other Pre-specified Outcome Measures | Not Provided | ||||||
Original Other Pre-specified Outcome Measures | Not Provided | ||||||
Descriptive Information | |||||||
Brief Title | Clinical and Laboratory Characteristics of Sickle Cell Anemia Patients Admitted With Fever | ||||||
Official Title | 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 | ||||||
Brief Summary | This study will summarized the clinical and laboratory data and the outcome of all the patients suffering from Sickle Cell Anemia (Including Sickle cell thalassemia) admitted to the pediatric ward. | ||||||
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. |
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Study Type | Observational | ||||||
Study Design | Time Perspective: Retrospective | ||||||
Target Follow-Up Duration | Not Provided | ||||||
Biospecimen | Not Provided | ||||||
Sampling Method | Probability Sample | ||||||
Study Population | 60 patients treated at the Pediatric Hematology Unit in the Ha'Emek Medical Center suffering from sickle cell anemia or sickle cell thalassemia admitted with fever as the presenting symptom. | ||||||
Condition |
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Intervention | Other: Observational
Summary of clinical and laboratory data
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Study Groups/Cohorts |
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Publications * | Not Provided | ||||||
* Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline. |
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Recruitment Information | |||||||
Recruitment Status | Completed | ||||||
Estimated Enrollment |
60 | ||||||
Original Estimated Enrollment | Same as current | ||||||
Actual Study Completion Date | November 2008 | ||||||
Primary Completion Date | Not Provided | ||||||
Eligibility Criteria | 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. |
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Sex/Gender |
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Ages | Child, Adult, Older Adult | ||||||
Accepts Healthy Volunteers | No | ||||||
Contacts | Contact information is only displayed when the study is recruiting subjects | ||||||
Listed Location Countries | Israel | ||||||
Removed Location Countries | |||||||
Administrative Information | |||||||
NCT Number | NCT00736060 | ||||||
Other Study ID Numbers | 0027-08-EMC | ||||||
Has Data Monitoring Committee | No | ||||||
U.S. FDA-regulated Product | Not Provided | ||||||
IPD Sharing Statement | Not Provided | ||||||
Current Responsible Party | Dr Koren Ariel, HaEmek Medical Center, Israel | ||||||
Original Responsible Party | Dr Koren Ariel - Pediatric Hematology Unit, Ha'Emek Medical Center - Afula - Israel | ||||||
Current Study Sponsor | HaEmek Medical Center, Israel | ||||||
Original Study Sponsor | Same as current | ||||||
Collaborators | Not Provided | ||||||
Investigators |
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PRS Account | HaEmek Medical Center, Israel | ||||||
Verification Date | August 2011 |