- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02732444
Erythrocytes Membrane Stability in COPD Patients in Long-Term Home Oxygen Therapy
Erythrocytes Membrane Stability in Chronic Obstructive Pulmonary Disease Patients in Long-Term Home Oxygen Therapy
Study Overview
Status
Conditions
Detailed Description
COPD is a major cause of illness and death worldwide, representing a significant economic and social cost. In the household, it causes concern, limited social life and leisure; commits the budget and shortens life. In the professional field, reduces productivity, anticipates the retirement and results in pension payments and benefits. In the area of health system, motivates repeated calls in emergency rooms, outpatient clinics and is a frequent cause of hospitalizations, which causes high costs for government and society. Most cases can be attributed to smoke.
COPD is often developed in middle-aged smokers with long time exposure which have a variety of other diseases related to smoking or aging. COPD itself has also significant extra-pulmonary effects (systemic) that lead to comorbid conditions. Nutritional abnormalities, weight loss and skeletal muscle dysfunction are well-recognized extrapulmonary effects of COPD and patients are at high risk for myocardial infarction, osteoporosis, respiratory infection, bone fractures, depression, sleep disorders, anemia and glaucoma.
Thus, this study aims to investigate the erythrocyte membranes stability in patients with COPD compared to healthy individuals, since the loss or damage of the red blood cells may be related to worsening gas exchange of patients and caused, for example, by increased oxidative stress observed in the disease mechanism of COPD patients, especially those with advanced lung disease.
Cross-sectional, observational study, which will be compared COPD patients with Advanced Lung disease using Long-Term Home Oxygen Therapy to healthy subjects to evaluate the presence of difference in membrane stability in the red blood cells as well as differences in pulmonary function tests, physical tests, laboratory analysis and presence of oxidative stress, as well as their quality of life.
The results obtained after analysis of erythrocyte membranes stability, as well as oxidative stress and functional and laboratory tests will be correlated, both in patients with COPD Long-Term Home Oxygen Therapy as the control group in order to establish relationships between variables and also compare between groups to determine the differences among them.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
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Minas Gerais
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Uberlandia, Minas Gerais, Brazil
- Hospital of clinics of the federal university of uberlândia
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
Control Group
- Patients without significant cardiorespiratory disease diagnosed, matched for age and body mass index to the group of COPD patients and APD in LTOT;
- Nonsmoker;
- Age group over 40 years old;
- Male gender;
- Acceptance to participate and agreement to sign the Informed Consent Term
COPD Group in LTOT
- Patients with COPD and APD in LTOT;
- Patients who do not have associated severe heart disease;
- Patients with no pulmonary exacerbations in the past four weeks;
- Male gender;
- Age group over 40 years old;
- Acceptance to participate and agreement to sign the Informed Consent Term
Exclusion Criteria:
- Patients with a disability or orthopedic disfunction that unable mobility or performance of physical tests;
- Patients using lipid-lowering drugs such as statins and fibrates;
- Patients or family / guardians who refuse to sign the Informed Consent Term
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
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COPD and APD patients in LTOT
• COPD and APD patients in LTOT
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Healthy Control
• Patients without significant cardiorespiratory disease, matched for age and body mass index with the other group.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
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Erythrocyte Osmotic Fragility Test (FSO)
Time Frame: 1 day
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The stability of erythrocytes is an inverse function of their osmotic fragility and can be measured by erythrocyte osmotic fragility test (FSO).
The test of the FSO provides four parameters for the cell stability of measurement: dX, H50, Amax and Amin.
Dx parameter expresses variation in salt concentration necessary to take intact erythrocytes (Amin) to a complete lysis state (Amax), with a 100% hemolysis.
Increased dX values expresses greater stability of erythrocytes.
The H50 parameter is related to the salt concentration required to produce 50% hemolysis.
H50 larger values expresses lower stability of erythrocytes.
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1 day
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
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Blood Sample Collection by venipuncture into test tubes (Vacutainer) containing specific anticoagulants for each dose
Time Frame: 1 day
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The analysis of the following parameters: hematological evaluation (complete blood count), serum levels of folic acid, cobalamin (vitamin B12), homocysteine, lipid profile, lactate dehydrogenase, serum iron, ferritin, transferrin capacity index, uric acid, glucose, albumin, reticulocytes, C-reactive protein (CRP), total bilirubin (TB), direct bilirubin (DB), indirect bilirubin (IB) and glycated hemoglobin (HbA1c).
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1 day
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The blood gases analysis will be performed by Radiometer Copenhagen ABL 330TM device
Time Frame: 1 day
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Will be obtained: potential hydrogen (pH); arterial oxygen tension (PaO2), arterial carbon dioxide tension (PaCO2); and arterial oxyhemoglobin saturation (SaO2).
The location and the puncture technique, sample handling and other technical considerations will be made according to the recommendation of specific guidelines of the Brazilian Thoracic Society.
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1 day
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Modified Medical Research Council (MMRC) Dyspnea Scale - Quality of Life Questionnaires
Time Frame: 1 day
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British Medical Research Council developed this scale in order to predict future risk of mortality.
The grades vary from 0 to 4, considering 0 better clinical condition and 4 worse health state.
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1 day
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COPD Assessment Test (CAT) - Quality of Life Questionnaires
Time Frame: 1 day
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The CAT consists of eight questions assessing cough, sputum, chest tightness, dyspnea, limitations in home activities, confidence in leaving home, sleep and energy.
For each item, the patient chooses only one answer option, whose score ranges from zero to five.
At the end of the test, the sum of the scores results in clinical impact of COPD, according to the stratification score of development study and validation of the CAT.
The results vary according to the range of the scores, ranked as follows in relation to the clinical impact: 6-10 points, light; 11-20, moderate; 21-30, severe; and 31-40, very serious.
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1 day
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Clinical COPD Questionnaire (CCQ) - Quality of Life Questionnaires
Time Frame: 1 day
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The CCQ is a self-administered questionnaire used routinely for clinical evaluation of COPD patients, but was also accepted as simple and a useful tool to be used in clinical trials evaluating response treatments and interventions.
It consists of 10 items that must be answered based on the last seven days of the patient, and the results indicates their clinical condition based on an intensity scale in which zero represents the minimum possible limitation or absence of breathlessness, and six maximum limitation possible.
The CCQ has three domains: symptoms, functional status and mental state.
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1 day
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Medical Outcome Study 36-item Short-Form Health Survey (SF-36) - Quality of Life Questionnaires
Time Frame: 1 day
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The SF-36 is a generic tool often used as a measure of health-related quality of life, easy to administer and understand, is composed of 36 items covering eight domains: physical functioning, role limitations due to physical health, pain, general health perception, vitality, social functioning, role limitations due to emotional problems and mental health.
It presents a score of 0 (zero) to 100, where zero corresponds to the worst general state of health and 100 corresponds to the best state of health.
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1 day
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St. George's Respiratory Questionnaire (SGRQ) - Quality of Life Questionnaires
Time Frame: 1 day
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The SGRQ is a 50-item questionnaire developed to measure health status (quality of life) in patients with diseases of airways obstruction.
It is self-administered and consists of three domains: symptoms, activity and impact of disease.
Each domain has a maximum possible score and the total is expressed as a percentage of that maximum, where values above 10% reflects changes on quality of life.
A minimum change in score of 4 units was established as clinically relevant after patient and clinician testing.
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1 day
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Airways questionnaire 20 (Aq-20) - Quality of Life Questionnaires
Time Frame: 1 day
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AQ20 is a specific questionnaire for obstructive respiratory diseases, consisting of only 20 questions, derived from a longer questionnaire: Asthma Quality of Life Questionnaire (AQLQ).
On its validation, it was compared to two other more complexes questionnaires (SGRQ and AQLQ) and showed good correlation with these instruments and clinical presentation of the patient.
It is self-administered and its great advantage is the short time required to answer it, only 4 minutes, and simplified answers (yes, no or not applicable).
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1 day
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Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Spirometry - Pulmonary Function Testing
Time Frame: 1 day
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The spirometric measures pre and post inhalation of 400 µg of salbutamol via metered-dose inhalers will be held in the system Clinical Pulmonary Function-Spirometry. Airflow is measured using a Pitot tube (PreVentPneumotachTM), with flow and volume, and a 3L syringe calibration performed daily, considering the temperature, the humidity and the local barometric pressure.
The volunteers completed at least three forced expiratory maneuvers and slow acceptable and at least two reproducible, according to the criteria of the Brazilian Thoracic Society.
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1 day
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Plethysmography - Pulmonary Function Testing
Time Frame: 1 day
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The measurements of static lung volumes will be taken using plethysmography with the Elite Platinum DX system (MGC, Minnesota, USA).
Consisting of the following elements: (A) a box with volume of 699 l, that becomes airtight by closing the door; (B) manometer to measure the pressure inside the box; (C) mouthpiece for breathing, consisting of flowmeter by pneumotachography; (D) manometer to measure the pressure in the mouth (equal to alveolar pressure in the absence of airflow and with an open glottis); and (E) of the airflow switch electrically controlled.
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1 day
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Carbon Monoxide Diffusion - Pulmonary Function Testing
Time Frame: 1 day
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DLCO (Carbon Monoxide Diffusion) examine the amount of carbon monoxide (CO) that diffuses from the pulmonary capillaries through alveolar-capillary barrier.
The system used for this evaluation will be Platinum Elite DX (MGC, Minnesota, USA), applying the modified Krogh technique (single breath).
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1 day
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Cardiopulmonary Exercise Testing (CPET) In Cycle Ergometry - Physical Tests
Time Frame: 1 day
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The system used is the Cardio 2 (MGC, Minnesota, USA), which consists of a flow module, a gas analyzer and a computer with the software "Breeze Suite 7.2".
This controls the ergometer and provides the graphical presentation and examination reports.
The gas analyzer determines, breath by breath, the mixed expired fraction of respiratory gases.
The analysis of the oxygen (O2) concentration is made using zirconium cell and analysis of the carbon dioxide (CO2) concentration is done in optical analyzer by absorption of infrared light.
This module is calibrated before each test, using a reference sample gas (21% of O2 in nitrogen balance) and calibration mixture (12% of O2 and 5% of CO2 in nitrogen balance of the mixture).
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1 day
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Six-Minute Walk Test - Physical Tests
Time Frame: 1 day
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The six-minute walk test (6MWT) is performed in accordance to the American Thoracic Society (ATS) guidelines.
The equipment required for the test are: timer, pulse oximeter, heart rate monitor, sphygmomanometer and stethoscope.
The tests will be conducted on a 30 meters enclosed corridor, free of obstacles, with chairs positioned at each of its ends, always by the same examiners who will be previously trained.
Participants will be instructed to walk as fasten as possible during six minutes, being encouraged with standardized phrases every minute.
If necessary, participants can rest, but the timer will remain on and they will be instructed to continue the test as soon as possible until the end of the sixth minute.
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1 day
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Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Flaviana Gomes, Federal University of Uberlandia
Publications and helpful links
General Publications
- Borg GA. Psychophysical bases of perceived exertion. Med Sci Sports Exerc. 1982;14(5):377-81.
- Montuschi P, Collins JV, Ciabattoni G, Lazzeri N, Corradi M, Kharitonov SA, Barnes PJ. Exhaled 8-isoprostane as an in vivo biomarker of lung oxidative stress in patients with COPD and healthy smokers. Am J Respir Crit Care Med. 2000 Sep;162(3 Pt 1):1175-7. doi: 10.1164/ajrccm.162.3.2001063.
- Finkel T, Holbrook NJ. Oxidants, oxidative stress and the biology of ageing. Nature. 2000 Nov 9;408(6809):239-47. doi: 10.1038/35041687.
- Aki H, Yamamoto M. Drug binding to human erythrocytes in the process of ionic drug-induced hemolysis. Flow microcalorimetric approaches. Biochem Pharmacol. 1991 Jan 1;41(1):133-8. doi: 10.1016/0006-2952(91)90021-v.
- Chasis JA, Mohandas N. Erythrocyte membrane deformability and stability: two distinct membrane properties that are independently regulated by skeletal protein associations. J Cell Biol. 1986 Aug;103(2):343-50. doi: 10.1083/jcb.103.2.343.
- Cooper RA. Abnormalities of cell-membrane fluidity in the pathogenesis of disease. N Engl J Med. 1977 Aug 18;297(7):371-7. doi: 10.1056/NEJM197708182970707. No abstract available.
- Cunha CC, Arvelos LR, Costa JO, Penha-Silva N. Effects of glycerol on the thermal dependence of the stability of human erythrocytes. J Bioenerg Biomembr. 2007 Aug;39(4):341-7. doi: 10.1007/s10863-007-9092-z. Epub 2007 Oct 5.
- McNeil PL, Steinhardt RA. Loss, restoration, and maintenance of plasma membrane integrity. J Cell Biol. 1997 Apr 7;137(1):1-4. doi: 10.1083/jcb.137.1.1. No abstract available.
- Nishimura K, Izumi T, Tsukino M, Oga T. Dyspnea is a better predictor of 5-year survival than airway obstruction in patients with COPD. Chest. 2002 May;121(5):1434-40. doi: 10.1378/chest.121.5.1434.
- Park HS, Kim SR, Lee YC. Impact of oxidative stress on lung diseases. Respirology. 2009 Jan;14(1):27-38. doi: 10.1111/j.1440-1843.2008.01447.x.
- Penha-Silva N, Firmino CB, de Freitas Reis FG, da Costa Huss JC, de Souza TM, de Freitas MV, Netto RC. Influence of age on the stability of human erythrocyte membranes. Mech Ageing Dev. 2007 Jul-Aug;128(7-8):444-9. doi: 10.1016/j.mad.2007.06.007. Epub 2007 Jun 28.
- Singer SJ, Nicolson GL. The fluid mosaic model of the structure of cell membranes. Science. 1972 Feb 18;175(4023):720-31. doi: 10.1126/science.175.4023.720.
- Office of the Surgeon General (US); Office on Smoking and Health (US). The Health Consequences of Smoking: A Report of the Surgeon General. Atlanta (GA): Centers for Disease Control and Prevention (US); 2004. Available from http://www.ncbi.nlm.nih.gov/books/NBK44695/
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- FUUberlandia 01/2016
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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