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Metformin in Chronic Obstructive Pulmonary Disease

Primary Purpose

Chronic Obstructive Pulmonary Disease

Status
Completed
Phase
Phase 4
Locations
United Kingdom
Study Type
Interventional
Intervention
Metformin
Placebo
Sponsored by
St George's, University of London
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Chronic Obstructive Pulmonary Disease focused on measuring Chronic obstructive pulmonary disease, COPD, metformin

Eligibility Criteria

35 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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

Sites / Locations

  • North Tees and Hartlepool NHS Trust
  • University Hospitals of Morecambe Bay NHS Trust
  • East Sussex Healthcare NHS Trust
  • Blackpool Teaching Hospitals NHS Trust
  • Lancashire Teaching Hospitals NHS Trust
  • Sherwood Forest Hospitals NHS Trust
  • Chelsea and Westminster Hospital
  • St George's Hospital
  • Freeman Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

Metformin

Placebo

Arm Description

Metformin 1 g twice daily for 28-35 days

Matched placebo capsules

Outcomes

Primary Outcome Measures

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

Secondary Outcome Measures

COPD Assessment Test score
Exacerbation of Chronic Pulmonary Disease Tool (EXACT) score
Time to discharge
Number of days from hospital admission to hospital discharge
Recurrent exacerbation, readmission, and death rate
Rates 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 period
Mean daily insulin use during hospitalisation period following study entry
Haemoglobin A1c
Mean haemoglobin A1c concentration
C-reactive protein concentration
Mean concentration of C-reactive protein in the blood
Body mass index
Waist circumference
Forced expiratory volume in 1 second
Mean forced expiratory volume in 1 second (FEV1) expressed as a percentage of predicted value
Fructosamine
Mean serum fructosamine concentration
Interleukin 6
Serum concentration of IL-6 (absolute value and change from baseline)
Interleukin 8
Serum concentration of IL-8 (absolute value and change from baseline)
Tumor necrosis factor alpha
Serum concentration of TNF-alpha (absolute value and change from baseline)
Interferon gamma
Serum concentration of IFN-gamma (absolute value and change from baseline)
8-isoprostane
Serum concentration of 8-isoprostane (absolute value and change from baseline)
Total carbonyl stress
Total carbonyl stress, measured in serum (absolute value and change from baseline)
Glutathione reduced vs oxidised
Glutathione reduced vs oxidised, measured in serum (absolute value and change from baseline)

Full Information

First Posted
November 23, 2010
Last Updated
May 6, 2015
Sponsor
St George's, University of London
Collaborators
Medical Research Council, British Lung Foundation
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1. Study Identification

Unique Protocol Identification Number
NCT01247870
Brief Title
Metformin in Chronic Obstructive Pulmonary Disease
Official Title
A Randomised, Double-blind, Placebo-controlled Trial of Metformin in Chronic Obstructive Pulmonary Disease (COPD) Exacerbations: a Pilot Study
Study Type
Interventional

2. Study Status

Record Verification Date
May 2015
Overall Recruitment Status
Completed
Study Start Date
January 2011 (undefined)
Primary Completion Date
March 2014 (Actual)
Study Completion Date
May 2014 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
St George's, University of London
Collaborators
Medical Research Council, British Lung Foundation

4. Oversight

Data Monitoring Committee
No

5. Study Description

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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Chronic Obstructive Pulmonary Disease
Keywords
Chronic obstructive pulmonary disease, COPD, metformin

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
52 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Metformin
Arm Type
Experimental
Arm Description
Metformin 1 g twice daily for 28-35 days
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Matched placebo capsules
Intervention Type
Drug
Intervention Name(s)
Metformin
Intervention Description
Metformin 1 g twice daily for 28-35 days
Intervention Type
Drug
Intervention Name(s)
Placebo
Intervention Description
Placebo
Primary Outcome Measure Information:
Title
Capillary glucose concentration
Description
The mean capillary glucose concentration during hospitalisation period following study entry, as a measure of both efficacy and safety.
Time Frame
During hospitalisation period
Secondary Outcome Measure Information:
Title
COPD Assessment Test score
Time Frame
Study entry, hospital discharge, and follow-up
Title
Exacerbation of Chronic Pulmonary Disease Tool (EXACT) score
Time Frame
Days 5, 10 and 28
Title
Time to discharge
Description
Number of days from hospital admission to hospital discharge
Time Frame
Hospital discharge
Title
Recurrent exacerbation, readmission, and death rate
Description
Rates of recurrent exacerbation (defined as treatment with antibiotics and/or systemic corticosteroids for breathlessness, cough or wheeze), readmission to hospital, or death
Time Frame
3 months
Title
Insulin requirement during hospitalisation period
Description
Mean daily insulin use during hospitalisation period following study entry
Time Frame
During hospitalisation period following study entry
Title
Haemoglobin A1c
Description
Mean haemoglobin A1c concentration
Time Frame
Follow-up (one month post study entry)
Title
C-reactive protein concentration
Description
Mean concentration of C-reactive protein in the blood
Time Frame
Days 7 and follow-up (one month)
Title
Body mass index
Time Frame
Follow-up (one month)
Title
Waist circumference
Time Frame
Follow-up (one month)
Title
Forced expiratory volume in 1 second
Description
Mean forced expiratory volume in 1 second (FEV1) expressed as a percentage of predicted value
Time Frame
At hospital discharge and follow-up (one month)
Title
Fructosamine
Description
Mean serum fructosamine concentration
Time Frame
At hospital discharge and follow-up (one month)
Title
Interleukin 6
Description
Serum concentration of IL-6 (absolute value and change from baseline)
Time Frame
At hospital discharge and follow-up (one month)
Title
Interleukin 8
Description
Serum concentration of IL-8 (absolute value and change from baseline)
Time Frame
At hospital discharge and follow-up (one month)
Title
Tumor necrosis factor alpha
Description
Serum concentration of TNF-alpha (absolute value and change from baseline)
Time Frame
At hospital discharge and follow-up (one month)
Title
Interferon gamma
Description
Serum concentration of IFN-gamma (absolute value and change from baseline)
Time Frame
At hospital discharge and follow-up (one month)
Title
8-isoprostane
Description
Serum concentration of 8-isoprostane (absolute value and change from baseline)
Time Frame
At hospital discharge and follow-up (one month)
Title
Total carbonyl stress
Description
Total carbonyl stress, measured in serum (absolute value and change from baseline)
Time Frame
At hospital discharge and follow-up (one month)
Title
Glutathione reduced vs oxidised
Description
Glutathione reduced vs oxidised, measured in serum (absolute value and change from baseline)
Time Frame
At hospital discharge and follow-up (one month)

10. Eligibility

Sex
All
Minimum Age & Unit of Time
35 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Emma H Baker, MBChB PhD
Organizational Affiliation
St George's, University of London
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Andrew W Hitchings, BSc MBBS
Organizational Affiliation
St George's Healthcare NHS Trust
Official's Role
Principal Investigator
Facility Information:
Facility Name
North Tees and Hartlepool NHS Trust
City
Hartlepool
State/Province
Cleveland
ZIP/Postal Code
TS24 9AH
Country
United Kingdom
Facility Name
University Hospitals of Morecambe Bay NHS Trust
City
Lancaster
State/Province
Cumbria
ZIP/Postal Code
LA9 7RG
Country
United Kingdom
Facility Name
East Sussex Healthcare NHS Trust
City
Hastings
State/Province
East Sussex
ZIP/Postal Code
TN37 7PT
Country
United Kingdom
Facility Name
Blackpool Teaching Hospitals NHS Trust
City
Blackpool
State/Province
Lancashire
ZIP/Postal Code
FY3 8NR
Country
United Kingdom
Facility Name
Lancashire Teaching Hospitals NHS Trust
City
Preston
State/Province
Lancashire
ZIP/Postal Code
PR2 9HT
Country
United Kingdom
Facility Name
Sherwood Forest Hospitals NHS Trust
City
Sutton-in-Ashfield
State/Province
Nottinghamshire
ZIP/Postal Code
NG17 4JL
Country
United Kingdom
Facility Name
Chelsea and Westminster Hospital
City
London
ZIP/Postal Code
SW10 9NH
Country
United Kingdom
Facility Name
St George's Hospital
City
London
ZIP/Postal Code
SW17 0QT
Country
United Kingdom
Facility Name
Freeman Hospital
City
Newcastle
ZIP/Postal Code
NE7 7DN
Country
United Kingdom

12. IPD Sharing Statement

Citations:
PubMed Identifier
27174882
Citation
Hitchings AW, Baker EH, Jones PW. Handling missing items in the Exacerbations of Chronic Pulmonary Disease Tool. Eur Respir J. 2016 Aug;48(2):564-6. doi: 10.1183/13993003.00269-2016. Epub 2016 May 12. No abstract available.
Results Reference
derived
PubMed Identifier
26917577
Citation
Hitchings AW, Lai D, Jones PW, Baker EH; Metformin in COPD Trial Team. Metformin in severe exacerbations of chronic obstructive pulmonary disease: a randomised controlled trial. Thorax. 2016 Jul;71(7):587-93. doi: 10.1136/thoraxjnl-2015-208035. Epub 2016 Feb 25.
Results Reference
derived

Learn more about this trial

Metformin in Chronic Obstructive Pulmonary Disease

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