Phase 2 Sickle Cell Disease Trial, Recruiting
Who may be able to join
AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI
Who might be able to join this trial:
- You are between 18 and 80 years old and have been diagnosed with sickle cell disease (any type, confirmed by a blood test)
- You are able to read and sign a consent form agreeing to take part in the study
- You are able to lie still on a special bone density scanning machine (called a DXA scanner)
- If you could potentially become pregnant, you must have a negative urine pregnancy test at the start of the study
Who may not be able to join:
- You are currently pregnant
- You are unable to give your own consent to take part in the study
- You are under 18 years old (children, teenagers, or infants are not eligible)
- You are currently in prison or a correctional facility
- You have been admitted to a hospital for any reason within the 2 weeks before joining the study
Important: Always verify eligibility with the trial site directly before applying.
Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.
Contact this trial
Principal Investigator: Oyebimpe O Adesina, MD, MS, UC Davis School of Medicine
Phone: (916) 460-2749
Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.
GP referral letter
Print a one-page summary to share with your doctor.
Trial details
Where this trial is recruiting
Primary endpoints
Recruitment and retention rates; Incidence of Treatment-Emergent Adverse Events as assessed by participant report; Pain assessed by the Adult Sickle Cell Quality of Life Measurement System (ASCQ-Me) Pain Impact questionnaire
Can't join this trial?
Data last synced from ClinicalTrials.gov: 28 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.