Skip to content

Metformin in Chronic Obstructive Pulmonary Disease

A Randomised, Double-blind, Placebo-controlled Trial of Metformin in Chronic Obstructive Pulmonary Disease (COPD) Exacerbations: a Pilot Study

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01247870
Enrollment
52
Registered
2010-11-24
Start date
2011-01-31
Completion date
2014-05-31
Last updated
2015-05-07

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

Conditions

Chronic Obstructive Pulmonary Disease

Keywords

Chronic obstructive pulmonary disease, COPD, metformin

Brief summary

The purpose of this study is to determine the effect of a tablet medication, called metformin, in flare-ups (exacerbations) of chronic obstructive pulmonary disease. The investigators believe that metformin may effectively control the blood sugar level during COPD exacerbations. This is important because there is evidence that a high blood sugar level during exacerbations may be linked with a worse prognosis. The investigators also think that metformin may have other potentially useful effects on inflammation, antioxidant levels, the effectiveness of steroid treatment, and recovery.

Detailed description

Does metformin lower the blood sugar level in patients suffering from exacerbations of chronic obstructive pulmonary disease (COPD)? COPD is the fourth leading cause of death worldwide, and a major cause of ill health. In the UK, it affects some 3.7 million people and causes over 30,000 deaths per year. It is usually, but not always, caused by smoking. Most people affected are over 65-years-old. Sufferers experience progressively worsening cough, sputum production, breathlessness and exercise limitation. This is punctuated by 'flare-ups' (exacerbations), when their symptoms worsen substantially. Approximately 25% of patients hospitalised for exacerbations die within a year, and over 50% within 5 years. There is a pressing need for new and improved treatments for COPD exacerbations. This study will assess the effect of metformin, a tablet medication, in COPD exacerbations. Metformin has been in common use for over 50 years in patients with diabetes, to lower the blood sugar level. In COPD exacerbations, the blood sugar level is often high, and the higher it is, the more likely the patient will have a poor outcome. This led us to speculate that lowering the sugar level with metformin may improve outcomes from COPD exacerbations. However, COPD and diabetes are quite different diseases, and the investigators do not know whether metformin will work as a sugar-lowering medicine in COPD exacerbations. The investigators need to confirm this before the investigators can perform larger studies to assess its effect on outcomes such as readmission and mortality rates. The investigators will test this medicine in a 1-month trial in patients hospitalised for COPD exacerbations. The target sample size is 69 patients, with a minimum of 48 patients required for primary endpoint analysis. Two-thirds of the patients will take metformin, and one-third a dummy (placebo) tablet. Neither the patients nor the researchers know who is taking which. The investigators will measure their sugar levels by regular finger-prick tests, and then compare the average readings in the two groups. The investigators will also assess the medicine's effects on other markers of blood sugar level, and carry out additional exploratory investigations on the effect of the medicine on clinical outcomes, markers of inflammation, and markers of oxidative/carbonyl stress and steroid responsiveness.

Interventions

DRUGMetformin

Metformin 1 g twice daily for 28-35 days

DRUGPlacebo

Placebo

Sponsors

Medical Research Council
CollaboratorOTHER_GOV
British Lung Foundation
CollaboratorOTHER
St George's, University of London
Lead SponsorOTHER

Study design

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

Eligibility

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

Inclusion criteria

* Diagnosis of COPD * Hospitalisation for exacerbation of COPD * Age ≥35 years * Expected to remain in hospital for at least 48 hours

Exclusion criteria

* Prior diagnosis of diabetes mellitus requiring insulin or oral hypoglycaemic therapy * Hypersensitivity to metformin hydrochloride or to any of the excipients * Renal impairment * Severe sepsis * Metabolic acidosis * Decompensated type 2 respiratory failure * Severe congestive cardiac failure * Acute coronary syndrome * Hepatic insufficiency * Excessive alcohol consumption * Malnourished or at high risk for malnutrition * Moribund or not for active treatment * Admitted to critical care unit * Unable to give informed consent * Pregnancy or lactation

Design outcomes

Primary

MeasureTime frameDescription
Capillary glucose concentrationDuring hospitalisation periodThe mean capillary glucose concentration during hospitalisation period following study entry, as a measure of both efficacy and safety.

Secondary

MeasureTime frameDescription
Exacerbation of Chronic Pulmonary Disease Tool (EXACT) scoreDays 5, 10 and 28
Time to dischargeHospital dischargeNumber of days from hospital admission to hospital discharge
Recurrent exacerbation, readmission, and death rate3 monthsRates of recurrent exacerbation (defined as treatment with antibiotics and/or systemic corticosteroids for breathlessness, cough or wheeze), readmission to hospital, or death
Insulin requirement during hospitalisation periodDuring hospitalisation period following study entryMean daily insulin use during hospitalisation period following study entry
Haemoglobin A1cFollow-up (one month post study entry)Mean haemoglobin A1c concentration
C-reactive protein concentrationDays 7 and follow-up (one month)Mean concentration of C-reactive protein in the blood
Body mass indexFollow-up (one month)
Waist circumferenceFollow-up (one month)
COPD Assessment Test scoreStudy entry, hospital discharge, and follow-up
FructosamineAt hospital discharge and follow-up (one month)Mean serum fructosamine concentration
Interleukin 6At hospital discharge and follow-up (one month)Serum concentration of IL-6 (absolute value and change from baseline)
Interleukin 8At hospital discharge and follow-up (one month)Serum concentration of IL-8 (absolute value and change from baseline)
Tumor necrosis factor alphaAt hospital discharge and follow-up (one month)Serum concentration of TNF-alpha (absolute value and change from baseline)
Interferon gammaAt hospital discharge and follow-up (one month)Serum concentration of IFN-gamma (absolute value and change from baseline)
8-isoprostaneAt hospital discharge and follow-up (one month)Serum concentration of 8-isoprostane (absolute value and change from baseline)
Total carbonyl stressAt hospital discharge and follow-up (one month)Total carbonyl stress, measured in serum (absolute value and change from baseline)
Glutathione reduced vs oxidisedAt hospital discharge and follow-up (one month)Glutathione reduced vs oxidised, measured in serum (absolute value and change from baseline)
Forced expiratory volume in 1 secondAt hospital discharge and follow-up (one month)Mean forced expiratory volume in 1 second (FEV1) expressed as a percentage of predicted value

Countries

United Kingdom

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 2, 2026