Impact of Roflumilast on Visceral Adiposity and Metabolic Profile in Chronic Obstructive Pulmonary Disease (RAMBO)
Primary Purpose
Chronic Obstructive Pulmonary Disease, Metabolic Syndrome
Status
Terminated
Phase
Phase 2
Locations
Canada
Study Type
Interventional
Intervention
Roflumilast
Placebo
Sponsored by
About this trial
This is an interventional treatment trial for Chronic Obstructive Pulmonary Disease focused on measuring COPD, Intrabdominal adiposity, Body composition, Triglycerides, Cholesterol
Eligibility Criteria
Inclusion Criteria:
- Gave an informed consent
- Forced expiratory volume in 1 second < 80% predicted
- Forced expiratory volume in 1 second / Forced vital capacity < 70%
- No exacerbation in the last 4 weeks
- Current or ex-smoker
- Smoking history of at least 10 pack/year
- Body mass index of at least 25 kg/m2
- Waist circumference of at least 94 cm
- Fasting blood triglycerides of at least 1.7 mmol/L
Exclusion Criteria:
- Any significant pulmonary pathology other than COPD
- Under oxygen therapy more than 12 hours per day
- More than 2 exacerbation episodes in the last 12 months
- The patient is currently participating to the active phase of a rehabilitation program
- Patient has been under roflumilast therapy prior to enrollment
- Unstable hypertriglyceridemia or hypercholesterolemia
- Under diabetes therapy (hypoglycemic agent or insulin)
- Cancer history in the last 5 years (except basal cell carcinoma)
- Moderate or severe hepatic impairment
- Used prednisone or systemic corticosteroids in the last 4 weeks
Sites / Locations
- St. Paul's Hospital
- Centre hospitalier de l'Université de Montréal
- Montreal Chest Institute
- Institut universitaire de cardiologie et de pneumologie de Québec
- Hôpital régional de Saint-Jérôme
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Placebo Comparator
Arm Label
Roflumilast
Placebo pill
Arm Description
Roflumilast 500 mcg, once daily for 6 months
Placebo pill, once daily for 6 months
Outcomes
Primary Outcome Measures
Change in intrabdominal adiposity
Measured by CT scan.
Secondary Outcome Measures
Change in body mass index
Change in waist circumference
Change in waist-to-hip circumference ratio
Change in blood metabolic profile
Blood glucose, insulin, triglycerides, apolipoprotein B, LDL/HDL cholesterol, C-reactive protein will be measured.
Change in body composition
As measured by dual-energy X-ray absorptiometry (DEXA).
Change in subcutaneous adiposity
As measured by CT scan.
Change in liver fat
As measured by CT scan
Full Information
NCT ID
NCT01701934
First Posted
October 3, 2012
Last Updated
November 10, 2014
Sponsor
Laval University
Collaborators
Innovair, Takeda
1. Study Identification
Unique Protocol Identification Number
NCT01701934
Brief Title
Impact of Roflumilast on Visceral Adiposity and Metabolic Profile in Chronic Obstructive Pulmonary Disease
Acronym
RAMBO
Official Title
Impact of Roflumilast on Visceral Adiposity and MetaBolic Profile in Chronic Obstructive Lung Disease: a Randomized and Controlled Trial: the RAMBO Trial.
Study Type
Interventional
2. Study Status
Record Verification Date
November 2014
Overall Recruitment Status
Terminated
Why Stopped
The recruitment of the study was prematurely stopped in July 2014 for the following reason; no more study medication.
Study Start Date
February 2013 (undefined)
Primary Completion Date
October 2014 (Actual)
Study Completion Date
December 2014 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Laval University
Collaborators
Innovair, Takeda
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
The purpose of this study is to determine whether roflumilast can improve metabolic profile and reduce visceral adiposity in patients with chronic obstructive pulmonary disease (COPD).
Detailed Description
Although underweight has been the traditional nutritional concern in patients with COPD, overweight and obesity are becoming important issues in this disease. In a rehabilitation study, investigators found that 66% of patients with moderate to severe COPD were either overweight or obese according to the WHO obesity classification (BMI ≥ 25 kg/m2). Obesity and COPD being two frequent conditions, it is important to understand the nature of their interactions.
Obesity, particularly in its visceral form is associated with a plethora of metabolic consequences that increases the risk of cardiovascular diseases. This would seem relevant to COPD which is in itself an important risk factor for cardiovascular diseases. The presence of obesity, particularly visceral obesity, may thus define in patients with COPD a clinical phenotype at high risk of cardiovascular diseases. In this context, it is relevant to note that the prevalence of metabolic syndrome is increased in COPD. Although fat distribution has not been precisely assessed in COPD studies, increased waist circumference is common in this disease suggesting that visceral obesity is part of the obesity syndrome seen in COPD.
Given the relationship between COPD, obesity and the metabolic syndrome and cardiovascular diseases, it is tempting to suggest that visceral obesity is likely to be frequent in COPD (as in the general population) and that the profound metabolic and inflammatory perturbations associated with this form of overweight/obesity could play a central role in the link between COPD and cardiovascular diseases.
Roflumilast, a Phosphodiesterase-4 inhibitor, has been recently evaluated as an anti-inflammatory medication in patients with COPD. Roflumilast, alone or in combination with long-acting bronchodilators, provide modest but significant improvement in lung function along with reductions in the rate of exacerbation in patients with moderate to severe COPD. A very interesting observation that was made in these 12-month duration studies was that the use of roflumilast was associated with an average reduction in body weight of 2 kg that took place during the first 6 months of the trials and remained relatively stable throughout the rest of the trials. The mechanisms and the precise effects of roflumilast on body composition and adipose tissue distribution have not been studied in great detail. However, available data suggest that roflumilast induces a preferential loss in body fat mass in comparison to fat-free mass. It remains to be seen whether roflumilast specifically affects visceral versus subcutaneous adipose tissue. The improved insulin sensitivity reported in one study in the presence of an apparently trivial weight loss (0.7 kg compared to placebo) may suggest that a selective loss of visceral adipose tissue may have been produced in response to roflumilast therapy.
These observations, although not definitive, suggest that roflumilast could be used not only to treat the respiratory component of COPD but also to modulate the metabolic aspect of this disease including visceral adiposity, features of the metabolic syndrome and significant co-morbidities of COPD.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Chronic Obstructive Pulmonary Disease, Metabolic Syndrome
Keywords
COPD, Intrabdominal adiposity, Body composition, Triglycerides, Cholesterol
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
14 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Roflumilast
Arm Type
Experimental
Arm Description
Roflumilast 500 mcg, once daily for 6 months
Arm Title
Placebo pill
Arm Type
Placebo Comparator
Arm Description
Placebo pill, once daily for 6 months
Intervention Type
Drug
Intervention Name(s)
Roflumilast
Other Intervention Name(s)
DAXAS
Intervention Description
500 mcg, oral, once daily for 6 months
Intervention Type
Drug
Intervention Name(s)
Placebo
Other Intervention Name(s)
Inactive comparator
Intervention Description
One placebo pill daily, for 6 months
Primary Outcome Measure Information:
Title
Change in intrabdominal adiposity
Description
Measured by CT scan.
Time Frame
At baseline and 6 months later
Secondary Outcome Measure Information:
Title
Change in body mass index
Time Frame
At baseline and 6 months later
Title
Change in waist circumference
Time Frame
At baseline and 6 months later
Title
Change in waist-to-hip circumference ratio
Time Frame
At baseline and 6 months later
Title
Change in blood metabolic profile
Description
Blood glucose, insulin, triglycerides, apolipoprotein B, LDL/HDL cholesterol, C-reactive protein will be measured.
Time Frame
At baseline and 6 months later
Title
Change in body composition
Description
As measured by dual-energy X-ray absorptiometry (DEXA).
Time Frame
At baseline and 6 months later
Title
Change in subcutaneous adiposity
Description
As measured by CT scan.
Time Frame
At baseline and 6 months later
Title
Change in liver fat
Description
As measured by CT scan
Time Frame
At baseline and 6 months later
10. Eligibility
Sex
Male
Minimum Age & Unit of Time
40 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Gave an informed consent
Forced expiratory volume in 1 second < 80% predicted
Forced expiratory volume in 1 second / Forced vital capacity < 70%
No exacerbation in the last 4 weeks
Current or ex-smoker
Smoking history of at least 10 pack/year
Body mass index of at least 25 kg/m2
Waist circumference of at least 94 cm
Fasting blood triglycerides of at least 1.7 mmol/L
Exclusion Criteria:
Any significant pulmonary pathology other than COPD
Under oxygen therapy more than 12 hours per day
More than 2 exacerbation episodes in the last 12 months
The patient is currently participating to the active phase of a rehabilitation program
Patient has been under roflumilast therapy prior to enrollment
Unstable hypertriglyceridemia or hypercholesterolemia
Under diabetes therapy (hypoglycemic agent or insulin)
Cancer history in the last 5 years (except basal cell carcinoma)
Moderate or severe hepatic impairment
Used prednisone or systemic corticosteroids in the last 4 weeks
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
François Maltais, MD
Organizational Affiliation
Institut universitaire de cardiologie et de pneumologie de Québec, University Laval
Official's Role
Principal Investigator
Facility Information:
Facility Name
St. Paul's Hospital
City
Vancouver
State/Province
British Columbia
ZIP/Postal Code
V6Z 1Y6
Country
Canada
Facility Name
Centre hospitalier de l'Université de Montréal
City
Montréal
State/Province
Quebec
ZIP/Postal Code
H2W 1T8
Country
Canada
Facility Name
Montreal Chest Institute
City
Montréal
State/Province
Quebec
ZIP/Postal Code
H2X 2P4
Country
Canada
Facility Name
Institut universitaire de cardiologie et de pneumologie de Québec
City
Québec
State/Province
Quebec
ZIP/Postal Code
G1V 4G5
Country
Canada
Facility Name
Hôpital régional de Saint-Jérôme
City
Saint-Jérôme
State/Province
Quebec
ZIP/Postal Code
J7Z 5T3
Country
Canada
12. IPD Sharing Statement
Citations:
PubMed Identifier
21054892
Citation
Sava F, Laviolette L, Bernard S, Breton MJ, Bourbeau J, Maltais F. The impact of obesity on walking and cycling performance and response to pulmonary rehabilitation in COPD. BMC Pulm Med. 2010 Nov 6;10:55. doi: 10.1186/1471-2466-10-55.
Results Reference
background
PubMed Identifier
17167477
Citation
Despres JP, Lemieux I. Abdominal obesity and metabolic syndrome. Nature. 2006 Dec 14;444(7121):881-7. doi: 10.1038/nature05488.
Results Reference
background
PubMed Identifier
12654609
Citation
Sin DD, Man SF. Why are patients with chronic obstructive pulmonary disease at increased risk of cardiovascular diseases? The potential role of systemic inflammation in chronic obstructive pulmonary disease. Circulation. 2003 Mar 25;107(11):1514-9. doi: 10.1161/01.cir.0000056767.69054.b3.
Results Reference
background
PubMed Identifier
16056071
Citation
Marquis K, Maltais F, Duguay V, Bezeau AM, LeBlanc P, Jobin J, Poirier P. The metabolic syndrome in patients with chronic obstructive pulmonary disease. J Cardiopulm Rehabil. 2005 Jul-Aug;25(4):226-32; discussion 233-4. doi: 10.1097/00008483-200507000-00010.
Results Reference
background
PubMed Identifier
19574332
Citation
Lam KB, Jordan RE, Jiang CQ, Thomas GN, Miller MR, Zhang WS, Lam TH, Cheng KK, Adab P. Airflow obstruction and metabolic syndrome: the Guangzhou Biobank Cohort Study. Eur Respir J. 2010 Feb;35(2):317-23. doi: 10.1183/09031936.00024709. Epub 2009 Jul 2.
Results Reference
background
PubMed Identifier
19716961
Citation
Fabbri LM, Calverley PM, Izquierdo-Alonso JL, Bundschuh DS, Brose M, Martinez FJ, Rabe KF; M2-127 and M2-128 study groups. Roflumilast in moderate-to-severe chronic obstructive pulmonary disease treated with longacting bronchodilators: two randomised clinical trials. Lancet. 2009 Aug 29;374(9691):695-703. doi: 10.1016/S0140-6736(09)61252-6.
Results Reference
background
PubMed Identifier
19716960
Citation
Calverley PM, Rabe KF, Goehring UM, Kristiansen S, Fabbri LM, Martinez FJ; M2-124 and M2-125 study groups. Roflumilast in symptomatic chronic obstructive pulmonary disease: two randomised clinical trials. Lancet. 2009 Aug 29;374(9691):685-94. doi: 10.1016/S0140-6736(09)61255-1. Erratum In: Lancet. 2010 Oct 2;376(9747):1146.
Results Reference
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Impact of Roflumilast on Visceral Adiposity and Metabolic Profile in Chronic Obstructive Pulmonary Disease
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