FindTrial
Sign In

Genetic patterns and clinical features of Duchenne Muscular Dystrophy in children-A one year study

Correlation of Genetic Spectrum of Children with Duchenne Muscular Dystrophy with Clinical Phenotype-A one-year Prospective Cohort study at a tertiary care centre - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2025/09/094170
Enrollment
41
Registered
2025-09-03
Start date
Unknown
Completion date
Unknown
Last updated
2025-09-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: G710- Muscular dystrophy

Interventions

Intervention1: Nil: Nil Intervention2: Nil: Nil

Sponsors

Jawaharlal Nehru Medical College KLE university
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Children diagnosed with Duchenne muscular dystrophy, either with MLPA or whole exome sequencing

Exclusion criteria

Exclusion criteria: Those children with DMD who are variant of unceratian significance(vus) nad have not provided consent for sanger sequencing

Design outcomes

Primary

MeasureTime frame
To correlate the genetic profile of children with DMD with the clinical phenotypeTimepoint: The study will be conducted over a span of one year—

Secondary

MeasureTime frame
To study the genetic spectrum of children with DMDTimepoint: The study will be conducted over a span of one year—

Countries

India

Contacts

Public ContactPeddireddy Harsha Vardhana Reddy

Jawaharlal Nehru Medical College, Belagavi,Karnataka

bhavana.d23@gmail.com9986157763

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026