High Dose Vitamin D for Sickle Cell Disease
CompletedPhase 2NCT01331148
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This study has no listed site in Canada in this snapshot. It is included as part of the worldwide chronic pain corpus.
Brief summary (from the registry)
Vitamin D deficiency (VDD) is very common among African American adolescents and adults in the US, ten times higher than is seen in Caucasians. VDD is also quite common in sickle cell disease (SCD). Both VDD and SCD can cause chronic pain, compression fractures, and muscle weakness. The investigators believe VDD may contribute to poor musculoskeletal health and chronic pain seen in pediatric SCD. In this study, the investigators aim to show that children and adolescents with SCD and chronic pain have lower levels of vitamin D compared to those without chronic pain. The investigators also aim to determine the clinical characteristics in SCD patients related to their vitamin D status. About 60 subjects (7 to 21 years old) will be enrolled on this study, 30 with chronic pain and 30 without chronic pain. The investigators will assess baseline characteristics including vitamin D levels, bone turnover rates (measured by C telopeptide blood levels \[CTx\]), markers of inflammation and oxidative stress levels in blood, baseline hemoglobin and other laboratory parameters, presence of abnormal bones on chest x-ray, pulmonary function, opioid analgesic use, overall muscle strength, quality of life and depression. To evaluate the impact of vitamin D replacement on these baseline characteristics, the investigators will randomize subjects to receive either placebo or high dose vitamin D for 6 weeks after which time the investigators will evaluate overall vitamin D status, muscle and bone health, depression, quality of life, pain status and use of opioid pain medications, inflammation and oxidative status comparing before and after treatment with high dose vitamin D. The investigators will give-at no cost to subjects-a daily supplement that will provide the recommended daily allowance of calcium and vitamin D that contains 500mg Calcium and 200IU vitamin D to subjects throughout the study period. Subjects will be in the study for 7 months and have five to six study visits.
Study details
- Official title
- Pilot Study of Vitamin D to Ameliorate Chronic Pain in Sickle Cell Disease
- Conditions
- Interventions
- Drug: Vitamin D
- Other: Placebo
- Sponsor
- Wake Forest University Health Sciences
- Collaborators
- Children's Healthcare of Atlanta; Emory University
- Start date
- 2009-02
- Primary completion
- 2011-12
- Sex
- All
- Age range
- from 7 Years to 21 Years
- Results posted
- Yes, on ClinicalTrials.gov
- Countries
- United States
- Total sites listed
- 1
Eligibility criteria
Show eligibility criteria (verbatim from the registry)
Inclusion Criteria: * all sickle cell genotypes including SS, SB0thal, SC, SB+Thal * Age 7-21 years old * Last PRBC transfusion \>30 days prior Exclusion Criteria: * chronic renal failure * chronic liver disease * recent hospitalization \<14 days * history of malignancy * serum calcium level as defined in protocol section D 2.2 * treatment with concommitant medications as defined in section D 2.2 of the protocol * known malabsorption or short gut syndrome or conditions associated with poor GI absorption * patients currently on high dose vitamin D therapy
Source: ClinicalTrials.gov (US National Library of Medicine), snapshot October 2026. Check the registry for current recruiting status. Record: https://clinicaltrials.gov/study/NCT01331148