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:
- People who have been diagnosed with Sickle Cell Disease (specific types include SS, SC, Sß-thalassemia, SD, or SOArab)
- People who are 12 years old or older
- People who have given their legal consent to take part in all parts of the study
Who may not be able to join:
- People who are under 12 years old
- People who are currently taking part in another clinical trial involving an experimental treatment
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: Enrico Novelli, MD, University of Pittsburgh
Phone: 412-916-3416
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
Dermal water content measurements in SCD participants at baseline state of health; Dermal water content measurements before fluid resuscitation in SCD participants with VOC or VOE; Dermal water content measurements after fluid resuscitation in SCD participants with VOC or VOE; Clinical dehydration assessments in SCD participants; Measurement of serum osmolality as a laboratory biomarker of dehydration in SCD participants; Measurement of hyperadhesion as a laboratory biomarker of dehydration in SCD participants; Measurement of elongation index as a cellular biomarker of dehydration in SCD parti...
Can't join this trial?
Data last synced from ClinicalTrials.gov: 26 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.