Skip to content

Assessment of Efficacy and Safety of Magnesium Glycinate in the Management of Selected Inflammatory Diseases

A Randomimized, double blind, Parallel group study to assess safety and efficacy of Magnesium Glycinate in the management of selected inflammatory disease like Asthma, COPD, Rheumatoid Arthritis and Osteoarthritis - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/07/071708
Enrollment
200
Registered
2024-07-31
Start date
Unknown
Completion date
Unknown
Last updated
2024-08-19

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

Conditions

Health Condition 1: J449- Chronic obstructive pulmonary disease, unspecified Health Condition 2: J454- Moderate persistent asthma Health Condition 3: M179- Osteoarthritis of knee, unspecified Health Condition 4: M059- Rheumatoid arthritis with rheumatoid factor, unspecified

Interventions

Intervention1: Standard therapy + Magnesium Glycinate: 400mg - oral - once daily for 1 year Control Intervention1: standard therapy + Placebo: 400mg - oral - once daily - for one year

Sponsors

M Maneesh Kumar Reddy
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients with hypomagnesemia (serum magnesium level below 1.6mg/dl) Age (above 18 years) Individuals willing to participate in study Patients on standard therapy managing their inflammatory disorders (Asthma, COPD, Rheumatoid Arthritis and Osteoarthritis) Both sex

Exclusion criteria

Exclusion criteria: Known allergy to the any of the drug investigated Currently using any magnesium related products Having any psychiatric illness Administering drugs that affect ADME of investigation product Presence of alcohol or drug dependence Evidence of renal or hepatic impairment Pregnant and lactating women Participation in any other clinical trials

Design outcomes

Primary

MeasureTime frame
C-Reactive Protein, Inflammatory Markers (TNF Alpha, IL-6, IL-10), Disease Activity ScoreTimepoint: 0 month, 3 month, 6 month, 9 month, 12 month

Secondary

MeasureTime frame
Serum Magnesium, Quality of Life, Medication Adherence, Adverse Drug Reactions, FEV1/FVC (Asthma & COPD), Ligamentous Laxity (Osteoarthritis), Rheumatoid Factor (Rheumatoid Arthritis) Timepoint: 0 month, 3 month, 6 month, 9 month, 12 month

Countries

India

Contacts

Public ContactDr MG Rajanandh

SRM College of Pharmacy

mgr@srmist.edu.in7598464723

Outcome results

None listed

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