Risk-based Therapy for Sickle Cell Anemia: A Feasibility Study
Primary Purpose
Sickle Cell Anemia
Status
Withdrawn
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
Hydroxyurea
Placebo
Sponsored by
About this trial
This is an interventional prevention trial for Sickle Cell Anemia
Eligibility Criteria
Inclusion Criteria:
- ages 6-12 months
- Sickle cell anemia (HbSS)
- steady state absolute reticulocyte count between 2-6 months is available in the medical record
Exclusion Criteria:
- receiving hydroxyurea or chronic monthly blood transfusions
- patient enrolled in preliminary study
Sites / Locations
- Children's National Medical Center
Arms of the Study
Arm 1
Arm 2
Arm Type
Placebo Comparator
Active Comparator
Arm Label
Sugar water
Hydroxyurea
Arm Description
Placebo arm
Treatment Arm
Outcomes
Primary Outcome Measures
Sickle Cell Clinical Change from Baseline to Study Completion ( 18 months)
Participants will be have a study visit at baseline and then every month for the 18 month duration of the study. Study visits will include a physical exam, laboratory monitoring and interval history to assess the change (if any) every 4 weeks of sickle cell complications.
Secondary Outcome Measures
Full Information
NCT ID
NCT02090296
First Posted
February 4, 2014
Last Updated
October 16, 2017
Sponsor
Children's National Research Institute
1. Study Identification
Unique Protocol Identification Number
NCT02090296
Brief Title
Risk-based Therapy for Sickle Cell Anemia: A Feasibility Study
Official Title
Reticulocyte as Risk Marker: Targeted Therapy for Infants With Sickle Cell Anemia
Study Type
Interventional
2. Study Status
Record Verification Date
October 2017
Overall Recruitment Status
Withdrawn
Why Stopped
Participant withdrew consent
Study Start Date
February 2014 (undefined)
Primary Completion Date
June 2015 (Actual)
Study Completion Date
June 2015 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Children's National Research Institute
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Sickle cell anemia (SCA) patients experience organ damage that begins at an early age and results in significant morbidity and early mortality. Although all SCA patients share the same genetic mutation, the clinical complications are highly variable with some patients experiencing frequent and severe complications, while others have few serious complications. If SCA severity could be predicted early in life, those patients at greatest risk for complications could receive treatment prior to the onset of organ damage. No general SCA severity predictor or one that can be informative early in life exists. The investigators preliminary research has identified the absolute reticulocyte count (ARC) as a potential early predictive risk marker for SCA complications in pediatric patients. A higher ARC between ages 2 and 6 months of age is associated with an increased risk of hospitalization in the first 3 years of life; the mean ARC for the 36 patients who were hospitalized for SCA complications was significantly higher than that of the remaining 23 in those who were not hospitalized. Moreover, total hospitalizations were nearly three times higher by age 2 years in those infants who had an ARC of > 200 than for those infants whose ARC was <200. The proposed study will determine if ARC can be used as a risk-stratifier in asymptomatic infants with SCA and ascertain its value in targeting hydroxyurea therapy to those infants at highest risk of SCA sequelae.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Sickle Cell Anemia
7. Study Design
Primary Purpose
Prevention
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
0 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Sugar water
Arm Type
Placebo Comparator
Arm Description
Placebo arm
Arm Title
Hydroxyurea
Arm Type
Active Comparator
Arm Description
Treatment Arm
Intervention Type
Drug
Intervention Name(s)
Hydroxyurea
Other Intervention Name(s)
Hydrea
Intervention Type
Other
Intervention Name(s)
Placebo
Other Intervention Name(s)
Sugar water
Primary Outcome Measure Information:
Title
Sickle Cell Clinical Change from Baseline to Study Completion ( 18 months)
Description
Participants will be have a study visit at baseline and then every month for the 18 month duration of the study. Study visits will include a physical exam, laboratory monitoring and interval history to assess the change (if any) every 4 weeks of sickle cell complications.
Time Frame
Every 4 weeks for the 18 months study duration
10. Eligibility
Sex
All
Minimum Age & Unit of Time
6 Months
Maximum Age & Unit of Time
12 Months
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
ages 6-12 months
Sickle cell anemia (HbSS)
steady state absolute reticulocyte count between 2-6 months is available in the medical record
Exclusion Criteria:
receiving hydroxyurea or chronic monthly blood transfusions
patient enrolled in preliminary study
Facility Information:
Facility Name
Children's National Medical Center
City
Washington, D.C.
State/Province
District of Columbia
ZIP/Postal Code
20010
Country
United States
12. IPD Sharing Statement
Learn more about this trial
Risk-based Therapy for Sickle Cell Anemia: A Feasibility Study
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