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Effect of Magnesium Supplementation in COPD

Daily Supplementation of Magnesium Citrate in Moderate-severe Chronic Obstructive Pulmonary Disease: a Randomized, Controlled, Double-blind Trial

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02680769
Enrollment
76
Registered
2016-02-12
Start date
2016-03-31
Completion date
2019-03-31
Last updated
2016-06-13

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

Conditions

Pulmonary Disease, Chronic Obstructive

Brief summary

Magnesium (Mg) is involved in several pathways that could be affected in chronic obstructive pulmonary diseases (COPDs), namely in the contractility and excitability of neuro-muscolar endothelial cells and low-grade inflammation, a typical state of COPD. In this sense, several randomized controlled trials (RCTs) confirmed a positive role of Mg in asthma since long-period oral supplementation of Mg leads to a clinical and spirometric improvement. Subjects with COPD seem to have a reduced bioavailability of Mg probably due to the use of drugs that may increase Mg losses (e.g. beta-agonists and cortisones), to a reduced dietary Mg intake, and heavy smoking. A recent study showed that the administration of endovenous or aerosol Mg sulphate with beta-agonists acutely improve maximum expiratory flow during COPD relapses as well as the prolonged treatment with endovenous sulphate Mg led to a reduction in pulmonary hyperinflation and increase in muscles involved in respiration, with a consequent clinical and instrumental improvement. These evidences suggest that a chronic supplementation with Mg could improve COPD in clinical and instrumental parameters, but, at the best of our knowledge, no study was available in this sense.

Interventions

DIETARY_SUPPLEMENT300 mg of citrate Mg

This group will take an oral supplementation of 300 mg of citrate magnesium

OTHERPlacebo

This group will take a placebo

Sponsors

University of Padova
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
TRIPLE (Subject, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Adults (\>18 years). * Moderate-severe COPD (FEV1 between 30-80% of theorical values).

Exclusion criteria

* Already taking magnesium or calcium supplementations. * Severe renal (creatinine clearance\< 30 ml/min) or hepatic decline or presence of other co-morbidities interfering with outcomes (e.g. dementia). * Hypermagnesemia (serum Mg\>1.85 mmol/L).

Design outcomes

Primary

MeasureTime frame
Change in forced expiratory volume in the 1st second between baseline and 6 months0-3-6 months

Countries

Italy

Contacts

Primary ContactGiuseppe Sergi, MD
giuseppe.sergi@unipd.it00390498218492

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 22, 2026