DMCRN-02-001: Assessing Pediatric Endpoints in DM1

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
AgeUp to 59
SponsorVirginia Commonwealth University

About this trial

The overall goal of the study is to establish valid clinical endpoint assessments for children with congenital myotonic dystrophy type 1 and develop biomarkers for the condition.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Age neonate to 3 years 11 months at enrollment.

A diagnosis of CDM, which is defined as children having symptoms of myotonic dystrophy in the newborn period (<30 days), such as hypotonia, feeding or respiratory difficulty, requiring hospitalization to a ward or to the neonatal intensive care unit for more than 72 hours; and a genetic test confirming an expanded trinucleotide (CTG) repeat in the DMPK gene in the child or mother. An expanded CTG repeat size in the child is considered greater than 200 repeats or E1-E4 classification (E1= 200-500, E2=500-1,000, E3=1,000-1,500, E4>1,500).

Guardian is willing and able to sign consent and follow study procedures

Disqualifiers

Any other non-DM1 illness that would interfere with the ability or results of the study in the opinion of the site investigator

Significant trauma within one month

Internal metal or devices (exclusion for DEXA component)

History of bleeding disorder or platelet count <50,000

Trial population

30 children with CDM

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

Not listed

Trial groups

50 Participants
are grouped into 1 trial group
Group A: Congenital Myotonic Dystrophy (CDM)

Trial outcomes

Primary outcomes

1

To evaluate motor milestone attainment in individuals with CDM and ChDM and compare to typically developing children

Milestone Assessment using Peabody definitions: This survey would ask parents to assess the age of motor milestones in days, months of infant age. Birth history, including prematurity, ventilatory status, and feeding problems would also be collected on the CRF. Feeding and ventilatory support, as well as height and weight will be collected at each study visit.

Time frame
Through study completion at 18 months

Secondary outcomes

1

Dysarthria Assessment

A blinded, standardized video assessment tabulating language milestones by a trained rater will be conducted at each visit.

Time frame
Through study completion at 18 months
2

Vineland

The Vineland will be administered by an interviewer to ensure standardized intake of data. This assessment will capture the adaptive function, including gross motor and fine motor, as reported by the parent proxy.

Time frame
Through study completion at 18 months
3

CCMDHI

The congenital and childhood myotonic dystrophy health index is a disease specific patient or proxy reported outcome measure specific to these conditions. The current study will utilize the proxy version.

Time frame
Through study completion at 18 months
4

Domain Delta

This assessment asks parents for global impression of change related to the baseline visit and will be used as an anchoring measure for the statistical analyses.

Time frame
Through study completion at 18 months

Other outcomes

1

Correlate the functional outcome measures with potential biomarkers in CDM.

Fine needle muscle biopsy:On the baseline visit, a fine needle aspirate will be performed. Biopsy will only be peformed once to minimize the risk. The procedure will be performed with local anesthesia (1% lidocaine without epinephrine and free of preservatives) of the vastus lateralis. Following lidocaine injection, a fine needle will be used to aspirate the quadriceps muscle to obtain a total of one aspirate. The aspirate will be flash frozen in liquid nitrogen. A similar procedure has been performed on adults with DM1, and the average biopsy yields sufficient tissue for RNA-Seq analysis.

Time frame
Baseline
2

Blood Sampling

DNA and RNA samples will be processed by Virginia Commonwealth University.

Time frame
Baseline, month 12, month 18
3

Muscle mass, DEXA

Lean muscle mass will be evaluated using serial DEXA scans as an exploratory endpoint. All sites will use a Hologic DEXA scanner. Investigators will evaluate whole body lean mass, left and right arm lean mass, and left and right leg lean mass. Particularly early in childhood, investigators would expect rapid changes in lean muscle mass. If there were a divergence between controls and subjects with CDM, this would provide evidence that CDM is a disorder of muscle maturity, as well as provide a potential biomarker.

Time frame
Baseline, month 12, month 18
4

World Health Organization (WHO) Motor Milestones

The WHO Motor Milestones is a set of 6 standardized motor milestones that include 1) Sitting without support, 2) Standing with assistance, 3) Hands-\&-knees crawling, 4) Walking with assistance, 5) Standing alone, and 6) Walking alone.

Time frame
Through study completion at 18 months

Sponsors and contacts

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