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Completed

NCT Number: NCT01247870

Metformin in Chronic Obstructive Pulmonary Disease

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.

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Key information

Age range

35 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 4

Primary location

North Tees and Hartlepool NHS Trust, Hartlepool, Cleveland, United Kingdom

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About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

metformin

Drug

Metformin 1 g twice daily for 28-35 days

Placebo

Drug

Placebo

Primary outcomes

  1. Capillary glucose concentration

    Time frame: During hospitalisation period

    The mean capillary glucose concentration during hospitalisation period following study entry, as a measure of both efficacy and safety.

Secondary outcomes

  1. COPD Assessment Test score

    Time frame: Study entry, hospital discharge, and follow-up

  2. Exacerbation of Chronic Pulmonary Disease Tool (EXACT) score

    Time frame: Days 5, 10 and 28

  3. Time to discharge

    Time frame: Hospital discharge

    Number of days from hospital admission to hospital discharge

  4. Recurrent exacerbation, readmission, and death rate

    Time frame: 3 months

    Rates of recurrent exacerbation (defined as treatment with antibiotics and/or systemic corticosteroids for breathlessness, cough or wheeze), readmission to hospital, or death

  5. Insulin requirement during hospitalisation period

    Time frame: During hospitalisation period following study entry

    Mean daily insulin use during hospitalisation period following study entry

  6. Haemoglobin A1c

    Time frame: Follow-up (one month post study entry)

    Mean haemoglobin A1c concentration

  7. C-reactive protein concentration

    Time frame: Days 7 and follow-up (one month)

    Mean concentration of C-reactive protein in the blood

  8. Body mass index

    Time frame: Follow-up (one month)

  9. Waist circumference

    Time frame: Follow-up (one month)

  10. Forced expiratory volume in 1 second

    Time frame: At hospital discharge and follow-up (one month)

    Mean forced expiratory volume in 1 second (FEV1) expressed as a percentage of predicted value

  11. Fructosamine

    Time frame: At hospital discharge and follow-up (one month)

    Mean serum fructosamine concentration

  12. Interleukin 6

    Time frame: At hospital discharge and follow-up (one month)

    Serum concentration of IL-6 (absolute value and change from baseline)

  13. Interleukin 8

    Time frame: At hospital discharge and follow-up (one month)

    Serum concentration of IL-8 (absolute value and change from baseline)

  14. Tumor necrosis factor alpha

    Time frame: At hospital discharge and follow-up (one month)

    Serum concentration of TNF-alpha (absolute value and change from baseline)

  15. Interferon gamma

    Time frame: At hospital discharge and follow-up (one month)

    Serum concentration of IFN-gamma (absolute value and change from baseline)

  16. 8-isoprostane

    Time frame: At hospital discharge and follow-up (one month)

    Serum concentration of 8-isoprostane (absolute value and change from baseline)

  17. Total carbonyl stress

    Time frame: At hospital discharge and follow-up (one month)

    Total carbonyl stress, measured in serum (absolute value and change from baseline)

  18. Glutathione reduced vs oxidised

    Time frame: At hospital discharge and follow-up (one month)

    Glutathione reduced vs oxidised, measured in serum (absolute value and change from baseline)

Sponsors and collaborators

Lead sponsor

St George's, University of London

Other

Collaborators

  • British Lung Foundation
  • Medical Research Council

Registry information

Official study title

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

Important dates

Study start
2011
Primary completion
2014
Study completion
2014
First posted
Nov 24, 2010
Registry last updated
May 7, 2015

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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