CLINICAL_TRIALS ClinicalTrials.gov record update

SLC13A5 Deficiency: a Prospective Natural History Study - Remote Only (International)

This page presents selected fields from the linked source record. It does not add a medical interpretation.

Record identity and dates

Source: ClinicalTrials.gov
Source record ID: NCT04681781
Title field or adapter rule: protocolSection.identificationModule.officialTitle
Ingested At: 2026-04-25T22:27:06.529474+00:00
Published At: 2024-11-22T00:00:00+00:00
Record Updated At: 2024-11-22
Timestamp Basis: source retrieval time was not retained by the feed adapter
Date limitation: source retrieval time was not retained by the feed adapter

protocolSection.conditionsModule.conditions: ["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"]
protocolSection.statusModule.lastUpdatePostDateStruct.date: "2024-11-22"
protocolSection.identificationModule.nctId: "NCT04681781"
protocolSection.identificationModule.officialTitle: "SLC13A5 Deficiency: a Prospective Natural History Study - Remote Only (International)"
protocolSection.statusModule.overallStatus: "ENROLLING_BY_INVITATION"
protocolSection.designModule.phases: []
protocolSection.statusModule.resultsFirstPostDateStruct.date: ""

Intervention details are not present in the imported fields for this record. No drug-condition relationship is inferred from co-listing.

This index keeps the source fields it imported; it may not contain the complete original record. Verify wording and context in the linked source.