# SLC13A5 Deficiency Natural History Study - Remote Only

> **NCT04681781** · — · ENROLLING_BY_INVITATION · sponsor: **TESS Research Foundation** · enrollment: 20 (estimated)

## Conditions studied

- Citrate Transporter Deficiency
- Epilepsy
- Rare Diseases
- Movement Disorders
- Genetic Disorder
- SLC13A5 Deficiency
- EIEE25
- Kohlschutter-Tonz Syndrome (non-ROGDI)
- 17p13.1 Deletions Confined to SLC13A5 Gene
- Citrate Transporter Disorder

## Interventions

_None listed._

## Key facts

- **NCT ID:** NCT04681781
- **Lead sponsor:** TESS Research Foundation
- **Sponsor class:** OTHER
- **Phase:** —
- **Study type:** OBSERVATIONAL
- **Status:** ENROLLING_BY_INVITATION
- **Start date:** 2021-03-01
- **Primary completion:** 2023-12-31
- **Final completion:** 2025-09-01
- **Target enrollment:** 20 (ESTIMATED)
- **Last updated:** 2024-11-22

## Collaborators

- [object Object]

## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT04681781

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT04681781, "SLC13A5 Deficiency Natural History Study - Remote Only". Retrieved via AI Analytics 2026-07-05 from https://api.ai-analytics.org/clinical/NCT04681781. Licensed CC0.

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