ICD D57ORPHA:232SCD

Sickle Cell Disease

Sickle Cell Disease is an inherited blood disorder in which red blood cells become rigid and sickle-shaped, blocking blood flow and causing severe pain, organ damage, and increased infection risk. It is most prevalent in people of African, Mediterranean, Middle Eastern, and South Asian descent. Australia has a growing population living with SCD, with newborn screening now expanding nationally.

853
Articles
868
Trials (2 AU)
Updated
5 April 2026
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Common Questions

What is Sickle Cell Disease?

Sickle Cell Disease is an inherited blood disorder in which red blood cells become rigid and sickle-shaped, blocking blood flow and causing severe pain, organ damage, and increased infection risk. It is most prevalent in people of African, Mediterranean, Middle Eastern, and South Asian descent. Australia has a growing population living with SCD, with newborn screening now expanding nationally.

How many clinical trials are available for Sickle Cell Disease?

RareWays currently indexes 868 clinical trials for Sickle Cell Disease, of which 164 are actively recruiting. Trial availability changes as new studies are registered — check the trials tab for current status.

Where does the research data for Sickle Cell Disease come from?

RareWays aggregates research from PubMed, Europe PMC, OpenAlex, and ClinicalTrials.gov. Data is updated regularly by Rocky, RareWays' automated research engine. All articles and trials link directly to their original sources.

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This information is for general awareness only.

For guidance specific to your situation, please speak with your healthcare team.