# SLC13A5 Deficiency Natural History Study - United States Only

> **NCT06144957** · — · ENROLLING_BY_INVITATION · sponsor: **TESS Research Foundation** · enrollment: 17 (estimated)

## Conditions studied

- Citrate Transporter Deficiency
- Epilepsy
- Rare Diseases
- Movement Disorders
- Genetic Disorder
- SLC13A5 Deficiency
- EIEE25
- Kohlschutter-Tonz Syndrome (Non-ROGDI)
- Citrate Transporter Disorder
- DEE25

## Interventions

_None listed._

## Key facts

- **NCT ID:** NCT06144957
- **Lead sponsor:** TESS Research Foundation
- **Sponsor class:** OTHER
- **Phase:** —
- **Study type:** OBSERVATIONAL
- **Status:** ENROLLING_BY_INVITATION
- **Start date:** 2021-12-01
- **Primary completion:** 2025-09-30
- **Final completion:** 2025-09-30
- **Target enrollment:** 17 (ESTIMATED)
- **Last updated:** 2025-08-05

## Collaborators

- [object Object]
- [object Object]
- [object Object]

## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT06144957

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT06144957, "SLC13A5 Deficiency Natural History Study - United States Only". Retrieved via AI Analytics 2026-06-02 from https://api.ai-analytics.org/clinical/NCT06144957. Licensed CC0.

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