Mitochondrial Encephalomyopathies and Mental Retardation: Investigations of Clinical Syndromes Associated With MtDNA Point Mutations

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Record identity and dates

Source

ClinicalTrials.gov

Source record ID

NCT01532791

Title field or adapter rule

protocolSection.identificationModule.officialTitle

Ingested At

2026-04-25T22:28:34.428818+00:00

Published At

2026-01-23T00:00:00+00:00

Record Updated At

2026-01-23

Timestamp Basis

source retrieval time was not retained by the feed adapter

Date limitation

source retrieval time was not retained by the feed adapter

Fields recorded by this source

protocolSection.conditionsModule.conditions

["MELAS or m.3243 A\u003eG Mitochondrial DNA Mutation Carrier"]

protocolSection.statusModule.lastUpdatePostDateStruct.date

"2026-01-23"

protocolSection.identificationModule.nctId

"NCT01532791"

protocolSection.identificationModule.officialTitle

"Mitochondrial Encephalomyopathies and Mental Retardation: Investigations of Clinical Syndromes Associated With MtDNA Point Mutations"

protocolSection.statusModule.overallStatus

"RECRUITING"

protocolSection.designModule.phases

[]

protocolSection.statusModule.resultsFirstPostDateStruct.date

""

Study condition terms

• MELAS or m.3243 A>G Mitochondrial DNA Mutation Carrier (protocolSection.conditionsModule.conditions)

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

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