Zinc Supplementation in Sickle Cell Disease: A Precursor to the Think Zinc for Bones Trial

Recruiting Phase 2 Interventional Study
Sickle Cell Disease
No Placebo Group Every participant receives an active treatment — no one gets a placebo. Prior Safety Data This treatment has already been tested in at least one earlier human trial.
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At a Glance
Age
15 – 40
Sex
Any
Trial phase
Phase 2
Study type
Interventional
Purpose
Other
Participants needed
34 (estimated)
Sponsor
University of California, San Francisco · Other
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About This Trial
The goal of this short term prospective Phase II study is to compare the effects of two alternate daily doses of zinc (25 and 40 mg/day) in 34 randomly assigned homozygous Sickle Cell Disease (SCD-SS) patients aged 15-40 years old. The main question it aims to answer is: Which biomarkers are most responsive to zinc supplementation, and what is the maximum tolerated zinc dose that induces the desir…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Age: ≥ 15.0 to ≤ 40.0 years * Diagnosis: SCD-SS or SCD-S Beta zero Thalassemia, in steady state (defined as a minimum of 2 weeks days following pain crisis) * Male or Female Exclusion Criteria: * Taking any supplement containing zinc and unable/willing to stop for 3 months p…
Contacts

Beth Anne Martin

480-793-2162

beth.martin@ucsf.edu

CONTACT

Ellen Fung, PhD

510-428-3885

ellen.fung@ucsf.edu

CONTACT