Phase 4 Sickle Cell Disease Trial, Recruiting NCT06979492 Sponsor: Emory University Condition: Sickle Cell Disease
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Phase 4 Sickle Cell Disease Trial, Recruiting

NCT06979492
Recruiting Phase 4

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 female
  • You have been diagnosed with sickle cell disease (any type, such as HbSS, HbSC, or HbSβ thalassemia)
  • You are 18 years of age or older
  • You are currently pregnant, between 6 and 20 weeks along
  • You are able to understand what the study involves and are willing to sign a consent form agreeing to take part
  • If you have private health insurance, your insurance company has given prior approval for blood transfusions

Who may not be able to join:

  • You were already receiving regular, scheduled blood transfusions before becoming pregnant
  • You have previously had a serious reaction to a blood transfusion called delayed hemolytic transfusion reaction (DHTR) with hyperhemolysis (confirm with trial site)
  • Your blood has antibodies that would make it very difficult to find suitable donor blood for transfusions
  • You are unable or unwilling to receive blood transfusions for personal, religious, or medical reasons
  • You are currently pregnant with triplets
  • You have a serious medical or mental health condition that, in your doctor's opinion, would prevent you from safely participating in a clinical trial

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.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 26 July 2026
Phase 4 trials study a drug that has already been approved, monitoring long-term safety and effectiveness in real-world use.

Contact this trial

Principal Investigator: Ross Fasano, MD, Emory University

Phone: 404-712-5227

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

Status
Recruiting
Phase
Phase 4
Registry
ClinicalTrials.gov
Start date
1 April 2026
Est. completion
1 May 2028

Where this trial is recruiting

🇺🇸 United States

Primary endpoints

Hospital admissions rate; Number of maternal emergency department (ED)/Acute care visits; Number of SCD-related complications per group; Number of participants with pregnancy related complications; Maternal death

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

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.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov