Dyspnea Assessment in Hemodialysis Patients

NCT ID: NCT03773991

Last Updated: 2024-08-15

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

7 participants

Study Classification

OBSERVATIONAL

Study Start Date

2019-03-29

Study Completion Date

2020-02-25

Brief Summary

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Shortness of breath is very common among patients on dialysis for kidney failure; however, its causes are often not understood. This study will explore the lungs and the heart of these patients to determine the causes of shortness of breath. The amount of salt in the body tissues, which tends to accumulate in dialysis patients and can also cause shortness of breath, will also be measured. Machines that exploit magnetic resonance, ultrasound and x-rays to take images of the body interior will be employed; in addition, breathing tests, questionnaires and blood tests will also be used. 20 patients on dialysis will be recruited and have two visits: one at the beginning of the study and one year later to observe any changes in the lungs, heart and salt accumulation over time.

Detailed Description

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Rationale:

The available evidence suggest that End-Stage Renal Disease (ESRD) and hemodialysis (HD) have harmful effects on the lungs; the investigators hypothesize that these recurring pulmonary insults, in an analogous way as recurring myocardial ischemic injury for the heart, cause long term impairment in the pulmonary parenchyma, airways and circulation. In addition, observational studies have reported that dyspnea is a common symptom among ESRD patients on chronic HD treatment; however, no study up to now has directly addressed the issue, so that the relationship between dyspnea and pulmonary involvement in the HD population remains poorly understood.

The aim of this study is to explore the pathophysiological basis of dyspnea in patients with end stage renal disease on chronic HD, by using state-of-the-art imaging and functional study techniques.

Study Design:

This is an exploratory study involving a single center recruiting patients from the prevalent dialysis population of London, Ontario. 20 patients on maintenance hemodialysis will be recruited. The patients will undergo imaging, functional studies and blood sampling at the Robarts Research Institute on a non-dialysis day, during the short interval in the dialysis schedule, at baseline and after one year.

Study Procedures:

Blood Collection: blood will be collected from a venous access for standard-of-care tests, uremia and inflammation biomarkers.

Dyspnea Assessment: dyspnea will be assessed with the following self-administered questionnaires: Modified Medical Research Council Breathlessness Scale, the University of California, San Diego Shortness of Breath Questionnaire Pulmonary Function Tests: spirometry and plethysmography pre and post salbutamol administration, carbon monoxide diffusion (DLCO) and the fractional exhaled nitric oxide (FeNO) will be evaluated.

Six Minute Walk Test: the subjects able to do so will perform a six minute walk test, their dyspnea and overall fatigue at baseline and at the end of the exercise will be evaluated using the Borg Scale.

Lung MRI: a proton MRI with ultrashort echo time (UTE) acquisition sequences for the study of lung parenchyma and lung water will be employed. Images will be acquired twice, both pre and post a bronchodilator (salbutamol) challenge.

Sodium MRI: a proton T1 weighted fast-low-angle-shot (FLASH)- sequence will be acquired to delineate the anatomy of the lower leg. Then, a sodium MRI study of the subjects' legs (\~5 cm below the knee) will be obtained with the custom-made sodium coil at 3.0 Tesla.

Water content will also be quantified using proton-MRI with fat-suppressed inversion recovery sequence with proton density contrast.

Chest CT: a high-resolution chest CT scan will be performed using a 64-slice CT scanner. A low radiation dose protocol will be employed. A qualitative and quantitative evaluation of pulmonary airways, blood vessels and parenchyma will be performed.

2D Transthoracic Echocardiography: images will be taken in the left lateral decubitus. Images and loops from standard parasternal long axis and short axis, subcostal, apical 4, 2 and 3- chamber views will be recorded and analyzed for: global longitudinal strain, left ventricular ejection fraction, left ventricular mass, left atrial volume, right ventricular diameter, right atrial volume, right ventricular wall thickness, tricuspid annular plane systolic excursion, pulmonary artery systolic pressure, E/A ratio, E/E' ratio at the basal interventricular septum, aortic, mitral, tricuspid and pulmonary valve qualitative and quantitative function.

Conditions

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Dyspnea; Uremic End Stage Renal Disease Chronic Lung Disease Chronic Heart Disease Hemodialysis-Induced Symptom Sodium Excess

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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Maintenance Hemodialysis Patients

Patients on chronic hemodialysis therapy due to end-stage renal disease.

* Proton Lung MRI
* Sodium MRI of the leg
* Chest CT
* Transthoracic Echocardiography
* Fractional Exhaled Nitric Oxide
* Six-Minute Walk Test
* Pulmonary Function Tests
* Blood sampling
* Self-administered dyspnea questionnaires

Lung MRI

Intervention Type DIAGNOSTIC_TEST

Proton Lung Magnetic Resonance Imaging

Sodium MRI

Intervention Type DIAGNOSTIC_TEST

Sodium Soft Tissue Magnetic Resonance Imaging

Chest CT

Intervention Type DIAGNOSTIC_TEST

High-resolution Quantitative Chest CT

Echocardiography

Intervention Type DIAGNOSTIC_TEST

Transthoracic 2D Speckle-Tracking Echocardiography

Fractional Exhaled Nitric Oxide

Intervention Type DIAGNOSTIC_TEST

Fractional Exhaled Nitric Oxide testing

Pulmonary Function Tests

Intervention Type DIAGNOSTIC_TEST

Spirometry and Plethysmography

Blood Sampling

Intervention Type DIAGNOSTIC_TEST

Blood testing for: standard-of-care, inflammatory biomarkers, uremic toxins

Six-Minute Walk Test

Intervention Type DIAGNOSTIC_TEST

Six-Minute Walk Test

Dyspnea Questionnaires

Intervention Type DIAGNOSTIC_TEST

Modified Medical Research Council; University of California, San Diego Shortness of Breath Questionnaire; Borg Scale

Interventions

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Lung MRI

Proton Lung Magnetic Resonance Imaging

Intervention Type DIAGNOSTIC_TEST

Sodium MRI

Sodium Soft Tissue Magnetic Resonance Imaging

Intervention Type DIAGNOSTIC_TEST

Chest CT

High-resolution Quantitative Chest CT

Intervention Type DIAGNOSTIC_TEST

Echocardiography

Transthoracic 2D Speckle-Tracking Echocardiography

Intervention Type DIAGNOSTIC_TEST

Fractional Exhaled Nitric Oxide

Fractional Exhaled Nitric Oxide testing

Intervention Type DIAGNOSTIC_TEST

Pulmonary Function Tests

Spirometry and Plethysmography

Intervention Type DIAGNOSTIC_TEST

Blood Sampling

Blood testing for: standard-of-care, inflammatory biomarkers, uremic toxins

Intervention Type DIAGNOSTIC_TEST

Six-Minute Walk Test

Six-Minute Walk Test

Intervention Type DIAGNOSTIC_TEST

Dyspnea Questionnaires

Modified Medical Research Council; University of California, San Diego Shortness of Breath Questionnaire; Borg Scale

Intervention Type DIAGNOSTIC_TEST

Eligibility Criteria

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Inclusion Criteria

* Age equal to or greater than 18 years.
* Dialysis vintage equal to or greater than 3 months.

Exclusion Criteria

* Smoking history of more than 10 packs/year.
* Active tobacco and/or cannabis smoking.
* Diagnosed chronic pulmonary disease.
* Severe heart failure (NYHA class IV)
* Active infection (including tuberculosis) or malignancy.
* Pregnancy.
* Inability to give consent or understand written information.
* Peripheral oxygen saturation (by pulse oxymetry) dropping below 80% when performing a 12-seconds breathhold.
* Inability to perform spirometry or plethysmography maneuvers.
* Inability to tolerate MRI due to patient size and/or known history of claustrophobia.
* Subject has an implanted mechanically, electrically or magnetically activated device or any metal in their body which cannot be removed, including but not limited to pacemakers, neurostimulators, biostimulators, implanted insulin pumps, aneurysm clips, bioprosthesis, artificial limb, metallic fragment or foreign body, shunt, surgical staples (including clips or metallic sutures and/or ear implants.).
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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London Health Sciences Centre Research Institute OR Lawson Research Institute of St. Joseph's

OTHER

Sponsor Role lead

Responsible Party

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Chris McIntyre

Professor of Medicine, Medical Biophysics and Paediatrics, University of Western Ontario. Director of The Lilibeth Caberto Kidney Clinical Research Unit, London Health Sciences Centre.

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Christopher W McIntyre, MD PhD

Role: PRINCIPAL_INVESTIGATOR

London Health Sciences Centre Research Institute OR Lawson Research Institute of St. Joseph's

Locations

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London Health Sciences Centre

London, Ontario, Canada

Site Status

Countries

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Canada

References

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Murtagh FE, Addington-Hall JM, Edmonds PM, Donohoe P, Carey I, Jenkins K, Higginson IJ. Symptoms in advanced renal disease: a cross-sectional survey of symptom prevalence in stage 5 chronic kidney disease managed without dialysis. J Palliat Med. 2007 Dec;10(6):1266-76. doi: 10.1089/jpm.2007.0017.

Reference Type BACKGROUND
PMID: 18095805 (View on PubMed)

Fairshter RD, Vaziri ND, Mirahmadi MK. Lung pathology in chronic hemodialysis patients. Int J Artif Organs. 1982 Mar;5(2):97-100.

Reference Type BACKGROUND
PMID: 7095887 (View on PubMed)

Zoccali C, Torino C, Tripepi R, Tripepi G, D'Arrigo G, Postorino M, Gargani L, Sicari R, Picano E, Mallamaci F; Lung US in CKD Working Group. Pulmonary congestion predicts cardiac events and mortality in ESRD. J Am Soc Nephrol. 2013 Mar;24(4):639-46. doi: 10.1681/ASN.2012100990. Epub 2013 Feb 28.

Reference Type BACKGROUND
PMID: 23449536 (View on PubMed)

Nascimento MM, Qureshi AR, Stenvinkel P, Pecoits-Filho R, Heimburger O, Cederholm T, Lindholm B, Barany P. Malnutrition and inflammation are associated with impaired pulmonary function in patients with chronic kidney disease. Nephrol Dial Transplant. 2004 Jul;19(7):1823-8. doi: 10.1093/ndt/gfh190. Epub 2004 May 18.

Reference Type BACKGROUND
PMID: 15150347 (View on PubMed)

Wallin CJ, Jacobson SH, Leksell LG. Subclinical pulmonary oedema and intermittent haemodialysis. Nephrol Dial Transplant. 1996 Nov;11(11):2269-75. doi: 10.1093/oxfordjournals.ndt.a027147.

Reference Type BACKGROUND
PMID: 8941589 (View on PubMed)

Bolignano D, Rastelli S, Agarwal R, Fliser D, Massy Z, Ortiz A, Wiecek A, Martinez-Castelao A, Covic A, Goldsmith D, Suleymanlar G, Lindholm B, Parati G, Sicari R, Gargani L, Mallamaci F, London G, Zoccali C. Pulmonary hypertension in CKD. Am J Kidney Dis. 2013 Apr;61(4):612-22. doi: 10.1053/j.ajkd.2012.07.029. Epub 2012 Nov 17.

Reference Type BACKGROUND
PMID: 23164943 (View on PubMed)

Barak M, Nakhoul F, Katz Y. Pathophysiology and clinical implications of microbubbles during hemodialysis. Semin Dial. 2008 May-Jun;21(3):232-8. doi: 10.1111/j.1525-139X.2008.00424.x. Epub 2008 Mar 18.

Reference Type BACKGROUND
PMID: 18363602 (View on PubMed)

Plesner LL, Warming PE, Nielsen TL, Dalsgaard M, Schou M, Host U, Rydahl C, Brandi L, Kober L, Vestbo J, Iversen K. Chronic obstructive pulmonary disease in patients with end-stage kidney disease on hemodialysis. Hemodial Int. 2016 Jan;20(1):68-77. doi: 10.1111/hdi.12342. Epub 2015 Aug 5.

Reference Type BACKGROUND
PMID: 26245152 (View on PubMed)

Pabst S, Hammerstingl C, Hundt F, Gerhardt T, Grohe C, Nickenig G, Woitas R, Skowasch D. Pulmonary hypertension in patients with chronic kidney disease on dialysis and without dialysis: results of the PEPPER-study. PLoS One. 2012;7(4):e35310. doi: 10.1371/journal.pone.0035310. Epub 2012 Apr 18.

Reference Type BACKGROUND
PMID: 22530005 (View on PubMed)

Herrero JA, Alvarez-Sala JL, Coronel F, Moratilla C, Gamez C, Sanchez-Alarcos JM, Barrientos A. Pulmonary diffusing capacity in chronic dialysis patients. Respir Med. 2002 Jul;96(7):487-92. doi: 10.1053/rmed.2002.1346.

Reference Type BACKGROUND
PMID: 12194631 (View on PubMed)

Kovacevic P, Stanetic M, Rajkovaca Z, Meyer FJ, Vukoja M. Changes in spirometry over time in uremic patients receiving long-term hemodialysis therapy. Pneumologia. 2011 Jan-Mar;60(1):36-9.

Reference Type BACKGROUND
PMID: 21545062 (View on PubMed)

McIntyre CW, Odudu A. Hemodialysis-associated cardiomyopathy: a newly defined disease entity. Semin Dial. 2014 Mar;27(2):87-97. doi: 10.1111/sdi.12197.

Reference Type BACKGROUND
PMID: 24738144 (View on PubMed)

Belem LC, Zanetti G, Souza AS Jr, Hochhegger B, Guimaraes MD, Nobre LF, Rodrigues RS, Marchiori E. Metastatic pulmonary calcification: state-of-the-art review focused on imaging findings. Respir Med. 2014 May;108(5):668-76. doi: 10.1016/j.rmed.2014.01.012. Epub 2014 Feb 6.

Reference Type BACKGROUND
PMID: 24529738 (View on PubMed)

Incalzi RA, Corsonello A, Pedone C, Battaglia S, Paglino G, Bellia V; Extrapulmonary Consequences of COPD in the Elderly Study Investigators. Chronic renal failure: a neglected comorbidity of COPD. Chest. 2010 Apr;137(4):831-7. doi: 10.1378/chest.09-1710. Epub 2009 Nov 10.

Reference Type BACKGROUND
PMID: 19903974 (View on PubMed)

Romoff MS, Keusch G, Campese VM, Wang MS, Friedler RM, Weidmann P, Massry SG. Effect of sodium intake on plasma catecholamines in normal subjects. J Clin Endocrinol Metab. 1979 Jan;48(1):26-31. doi: 10.1210/jcem-48-1-26. No abstract available.

Reference Type BACKGROUND
PMID: 422701 (View on PubMed)

Other Identifiers

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110256

Identifier Type: -

Identifier Source: org_study_id

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