# Spanish Natural History Study for LAMA2 Muscular Dystrophy

> **NCT06924125** · — · RECRUITING · sponsor: **Hospital Universitari Vall d'Hebron Research Institute** · enrollment: 100 (estimated)

## Conditions studied

- LAMA2-MD (Merosin Deficient Congenital Muscular Dystrophy, MDC1A)
- Merosin Deficient CMD (Full or Partial)
- Merosin Deficient Congenital Muscular Dystrophy
- Muscular Dystrophies
- Cohort Studies

## Interventions

- **DIAGNOSTIC_TEST:** Motor function scales
- **DIAGNOSTIC_TEST:** MUSCLE ULTRASOUND
- **DIAGNOSTIC_TEST:** Muscle Elastography
- **OTHER:** Complete physical examination
- **OTHER:** Ventilatory/ respiratory and other support assessment
- **OTHER:** Oromotor function and nutrition
- **OTHER:** Motor Milestone Assessments

## Key facts

- **NCT ID:** NCT06924125
- **Lead sponsor:** Hospital Universitari Vall d'Hebron Research Institute
- **Sponsor class:** OTHER
- **Phase:** —
- **Study type:** OBSERVATIONAL
- **Status:** RECRUITING
- **Start date:** 2021-07-27
- **Primary completion:** 2030-07-01
- **Final completion:** 2030-07-01
- **Target enrollment:** 100 (ESTIMATED)
- **Last updated:** 2025-04-11

## Collaborators

- [object Object]

## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT06924125

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT06924125, "Spanish Natural History Study for LAMA2 Muscular Dystrophy". Retrieved via AI Analytics 2026-06-23 from https://api.ai-analytics.org/clinical/NCT06924125. Licensed CC0.

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