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SLC13A5 Deficiency Natural History Study - United States Only | Clinical Trials | Clareo Health

Enrolling By InvitationNCT06144957

SLC13A5 Deficiency Natural History Study - United States Only

SLC13A5 deficiency (Citrate Transporter Disorder, EIEE 25) is a rare genetic disorder with neurodevelopmental delays and seizure onset in the first few days of life. This natural history study is desi...

Lead sponsor: TESS Research Foundation•3 U.S. locations•View source on ClinicalTrials.gov

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Data from ClinicalTrials.govLast updated on ClinicalTrials.gov: August 5, 2025Terms

Trial snapshot

StatusENROLLING_BY_INVITATION

Phase—

Enrollment17

Start dateDec 2021

Last updatedAug 5, 2025

Condition

Citrate Transporter Deficiency Epilepsy Rare Diseases Movement Disorders Genetic Disorder+5 more

Locations shown

Lucille Packard Children's Hospital, Stanford University

Palo Alto, California

Brown University

Providence, Rhode Island

University of Texas Southwestern Dallas

Dallas, Texas

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Data Source & Attribution

This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.

ClinicalTrials.gov last update: August 5, 2025Data synced to Clareo: May 10, 2026

Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.

Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.

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