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Ayurveda based study to improve the quality of life in children with Duchenne Muscular Dystrophy

Ayurveda based approach to improve the quality of life in children with Duchenne Muscular Dystrophy - ARDMD

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2020/07/026906
Enrollment
75
Registered
2020-07-29
Start date
Unknown
Completion date
Unknown
Last updated
2026-01-12

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: Ayurveda Intervention: RASNASAPTAKAM KASHAYAM,RASNADI KASHAYAM (B), VIDARYADI KASHAYAM, BARANGYADI KASHAYAM(B,RASNAERANDADHI KASHAYAM,BADRADARWADI KASHAYAM,INDUKATHAM KASHAYAM,VARANADI

Sponsors

Molecular DiagnosticsCounseling care and Research CentreMDCRC
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Molecularly confirmed with DMD/BMD 2. Those who voluntarily opt for Ayurveda and have been devoid of steroids in past six month 3. At least 50 patient are ambulant at the time of enrollment 4. The expected age range of the participants with DMD is 3 to 15 years and the participants with BMD is 5 to 25 years of age 5. Able to comply with functional testing instruction 6. Written informed consent for active participants

Exclusion criteria

Exclusion criteria: 1. Without molecular diagnosis for Duchenne 2. Types of muscular dystrophy other than DMD/BMD 3. Under steroids currently 4. Not willing to participate in the study

Design outcomes

Secondary

MeasureTime frame
The below is applicable both to ambulant and non ambulant kid) 1. Range of motion - Goniometer 2. Cobb’s angle 3. % forced vital capacity (%FVC) 4. % Left ventricular Ejection Fraction 5. Wechslr’s scale 6. Weight for age 7. Barthel score / Functional independence measure 8. Peds QL 4.0 score Timepoint: 6 months once

Primary

MeasureTime frame
1.North Star Ambulatory Assessment / Egens’s Klassification 2.MRC Scale Primary outcome measure can be determined by 10-meter walk test of the individuals without assistance, time taken to climb 10 stairs and time to get up from supine position. (The above are for Children who are Ambulant) Timepoint: 6 months once

Countries

India

Contacts

Public ContactDrReji Joseph

AVP Research Foundation

drsomit.kumar@gmail.com9790502037

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: May 22, 2026