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Beta-1,3-1,6-Glucan to improve muscular dystrophy

Linear Clinical Study to Evaluate the Anti-Inflammatory and Beneficial Effects of Beta-1, 3-1, 6-Glucan, on another Muscular Dystrophy other than LGMD Patients

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/03/106491
Enrollment
12
Registered
2026-03-18
Start date
Unknown
Completion date
Unknown
Last updated
2026-03-30

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

Conditions

Health Condition 1: M638- Disorders of muscle in diseases classified elsewhere

Interventions

Intervention1: Standard of care with beta-1,3-1,6-Glucan: It has been proven to have the potent anti-inflammatory properties.Dose:Food Supplement Administration, once in oral route. Control Interventi

Sponsors

Muthulakshmikadalraja Charitable Trust
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Subject who diagnosed with another muscular dystrophy other than Limb-girdle Muscular Dystrophy (LGMD) 2.Male and Female subjects of age in between 3 years to 70 years 3.Subjects and legally authorized representative for vulnerable subjects must be willing to participate in the study and provide a written informed consent 4.Subject willing to and able to comply with the protocol

Exclusion criteria

Exclusion criteria: 1.Subject participated in another clinical trial in the last 30 days. 2.Subjects and legally authorized representative for vulnerable subjects who has not given informed consent for this study 3.Subjects with history of multiple sclerosis 4.Subjects with history of any muscular atrophy 5.Pregnant and lactating females

Design outcomes

Primary

MeasureTime frame
Observation of changes in the levels of IL-6 and Myoglobin urea from the baseline.Timepoint: 24 weeks

Secondary

MeasureTime frame
1.Measurement of the levels of CK, Titin, TNF, Haptoglobin, Dystrophin level, LFT, CBC, Cystatin C 2.Immunological Parameters: IL-13, CD-40, ESR 3.Muscle function assessments Timepoint: Day 30 3,Day 60 3,Day 90 3,Day 120 3,Day 180 3 and Monitoring Adverse events each visits

Countries

India

Contacts

Public ContactDr Raghavan Kadalraja

RK Maples Hospital

drkraghavan27@gmail.com9840301991

Outcome results

None listed

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