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 an adult woman
- You have been pregnant at some point, for any length of time
- You are willing to sign a consent form agreeing to take part
- You may have had one or more pregnancies (first-time or experienced mothers are both welcome)
- You are covered by health insurance
- (For the patient group) You have a wound/ulcer on your skin caused by poor blood circulation, diabetes, or sickle cell disease, or a combination of these
- (For the comparison/control group) You are a healthy volunteer of a similar age with no skin ulcers
Who may not be able to join:
- You are under 18 years old (for the patient group)
- You are under any form of legal protection, such as a court order, curatorship, or guardianship (for the patient group)
- You have a weakened immune system for any reason
- You do not wish to give your consent to take part
- You are unwilling to provide blood and/or saliva samples for yourself or a family member
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: Sélim ARACTINGI, MD, PHD, Dermatology unit, Cochin Hospital - APHP
Phone: 00 33 1 58 41 18 13
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
Transcriptomic analysis by single cell sequencing
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.