CLINICAL_TRIALS ClinicalTrials.gov record update

National Registry of Myotonic Dystrophy and Facioscapulohumeral Muscular Dystrophy Patients and Family Members

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: NCT00082108
Title field or adapter rule: protocolSection.identificationModule.officialTitle
Ingested At: 2026-04-25T22:27:11.851407+00:00
Published At: 2025-10-15T00:00:00+00:00
Record Updated At: 2025-10-15
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: ["Myotonic Dystrophy", "Facioscapulohumeral Muscular Dystrophy", "Muscular Dystrophy", "Myotonic Dystrophy Type 1", "Myotonic Dystrophy Type 2", "Congenital Myotonic Dystrophy", "PROMM (Proximal Myotonic Myopathy)", "Steinert\u0027s Disease", "Myotonic Muscular Dystrophy"]
protocolSection.statusModule.lastUpdatePostDateStruct.date: "2025-10-15"
protocolSection.identificationModule.nctId: "NCT00082108"
protocolSection.identificationModule.officialTitle: "National Registry of Myotonic Dystrophy and Facioscapulohumeral Muscular Dystrophy Patients and Family Members"
protocolSection.statusModule.overallStatus: "RECRUITING"
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.

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