Effect of CPAP in the Worsening of Renal Function in Early Stages of Chronic Kidney Disease (CKD) (Renas)
Primary Purpose
Chronic Kidney Insufficiency, Sleep Apnea
Status
Unknown status
Phase
Not Applicable
Locations
Spain
Study Type
Interventional
Intervention
CPAP
conservative treatment
Sponsored by
About this trial
This is an interventional treatment trial for Chronic Kidney Insufficiency focused on measuring CPAP, Chronic kidney disease, sleep apnea
Eligibility Criteria
Inclusion Criteria:
- Patients referred to the outpatient nephrology department with a diagnosis of chronic kidney disease stages G1-3 KDIGO
- Older than18 years
- Habitual snoring or observed apneas
- Scale sleep sleepiness (Epworth Test) with 11 points or lower.
Exclusion Criteria:
- Very debilitating chronic or neoplastic disease
- Respiratory failure (PaO 2 <55 mm Hg).
- Other symptoms of suspected sleep disorder different from OSAS.
- Patients unable to perform self-administered questionnaires.
- Patients with> 50% of central apnea or Cheyne-Stokes.
- Patients who do not sign the informed consent.
Sites / Locations
- Jaime CorralRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
cpap group
control group
Arm Description
CPAP treatment plus conservative treatment with lifestyle modifications.
Conservative treatment with lifestyle modifications.
Outcomes
Primary Outcome Measures
To test whether treatment with CPAP in patients with moderate to severe OSAS and CKD in stages KDIGO G1-3, reduces the progression of renal disease (30% drop in GF) after 2 years of followed up.
Number of participants with chronic kidney disease (CKD) and obstructive sleep apnea syndrome (OSAS) with a 30% decline in estimated glomerular filtration rate (eGFR) using the CKD-EPI (CKD Epidemiology Collaboration) 2009 creatinine equation after 2 years of followed up (each patient will be followed up for at least 2 years - range from 2 to 3 years)
Secondary Outcome Measures
To estimate the prevalence of OSAS in patients with CKD stages G1-3 KDIGO
Number of participants with CKD and snoring and observed apneas with an apnea and hypoapnea index (AHI) ≥15/hour in home-based polysomnography.
To test whether treatment with CPAP reduces the albumin / creatinine ratio in urine.
Number of participants with CKD and OSAS with a decline in urine albumin to creatinine ratio.
To evaluate whether treatment with CPAP reduces serum Cystatin C
Number of participants with CKD and OSAS with a decline in serum cystatin C levels
To evaluate whether treatment with CPAP reduces inflammation-endothelial disfunction markers
Number of participants with CKD and OSAS with a decline in inflammation-endothelial disfunction markers (interleukine-6, interleukine-8, reactive C protein, sedimentation rate, asymmetric dimethylaginine or ADMA, intercellular adhesion molecule 1 or ICAM-1, vascular adhesion protein 1 or VCAM 1, vascular endothelial growth factor or VEGF)
Evaluate whether treatment with CPAP reduces the progression of CKD to a different stage
number of participants with CKD and OSAS with a change to a higher CKD stage according to eGFR.
to test wheather CPAP reduces the percentage of patients achieving replacement therapy
number of participants with CKD and OSAS who need renal replacement therapy (haemodialysis, peritoneal dialysis or renal transplantation)
Evaluate wheather treatment with CPAP reduces the incidence of cardiovascular events
number of participants with CKD and OSAS who suffered a cardiovascular event (myocardial infarction, stroke, hospitalization for heart failure, atrial fibrillation)
Evaluate wheather treatment with CPAP reduces the mortality
number of participants with CKD and OSAS with CPAP treatment who died (all-cause mortality)
Evaluation of the cost-effectiveness of treatment groups with and without CPAP
Cost-effectiveness of treatment groups conducting a cost-effectiveness study that allow us to estimate the incremental cost-effectiveness ratio (ICER) of CPAP treatment group compared to the conventional treatment group
Compare the evolution of inflammation-endothelial disfunction markers in NO-OSAS group versus OSAS group
Number of participants with NO-OSAS versus OSAS who have a decline in inflammation-endothelial disfunction markers (interleukine-6, interleukine-8, reactive C protein, sedimentation rate, asymmetric dimethylaginine or ADMA, intercellular adhesion molecule 1 or ICAM-1, vascular adhesion protein 1 or VCAM 1, vascular endothelial growth factor or VEGF)
Compare the worsening of the glomerular filtration in NO OSAS group versus OSAS group
number of participants with NO OSAS versus OSAS who have a worsening of the glomerular filtration.
Compare the percentage of patients achieving renal replacement therapy in NO OSAS group versus OSAS group
number of participants who need renal replacement therapy in NO OSAS group versus OSAS group
Full Information
NCT ID
NCT03319888
First Posted
September 23, 2016
Last Updated
March 5, 2018
Sponsor
Sociedad Española de Neumología y Cirugía Torácica
1. Study Identification
Unique Protocol Identification Number
NCT03319888
Brief Title
Effect of CPAP in the Worsening of Renal Function in Early Stages of Chronic Kidney Disease (CKD)
Acronym
Renas
Official Title
Effect of CPAP in the Worsening of Renal Function in Early Stages of Chronic Kidney Disease (CKD)
Study Type
Interventional
2. Study Status
Record Verification Date
October 2017
Overall Recruitment Status
Unknown status
Study Start Date
November 20, 2017 (Actual)
Primary Completion Date
November 20, 2019 (Anticipated)
Study Completion Date
May 20, 2020 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Sociedad Española de Neumología y Cirugía Torácica
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
Objectives: Evaluate the effect of CPAP to reduce the progression of chronic kidney disease or CKD (the decline of glomerular filtration rate is ≥ 30%) in patients with early-stage renal disease and sleep apnea syndrome (OSAS). Other objectives are; determine the prevalence of OSAS in patients with early-stage renal disease and evaluate the changes in inflamatories markers and endothelial damage, the state of KDIGO, cardiovascular events, mortality and cost-effectiveness analysis in CPAP group versus non-CPAP group patients.
Methods: A prospective, multicentric, randomized and controlled study will be carried out for 3 years. Early-stage renal disease (G1-3 KDIGO) and OSAS patients will be included. The investigators will make a respiratory polygraphy to determinate OSAS (AHI ≥15/h) and after that, the investigators randomized patients in 2 groups; CPAP group and control group (non-CPAP treatment). Patients with AHI <15/h (non-OSAS) will be the reference group and the half of these patients, randomly chosen, will be followed up at the end of the follow up.
Statistic analysis: the investigators will analyze the differences in glomerular filtration rate before and after the treatment, comparing the percentage of patients with CKD progression for both groups. The investigators will use the chi square test with raw data and adjusted for confounding variables using intention to treat analysis with imputation of missing values.
Detailed Description
There is a bidirectional involvement between the chronic kidney disease (CKD) and sleep apnea syndrome (OSAS). The declining of renal function, the fluid overloading and the disturbance of ventilation control could cause sleep apneas. On the other hand, the nocturnal hypoxia in patients with OSAS has been associated with changes in the renin-angiotensin system and sympathetic nervous system and production of reactive oxygen species. These findings are relationed with the deterioration of kidney function.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Chronic Kidney Insufficiency, Sleep Apnea
Keywords
CPAP, Chronic kidney disease, sleep apnea
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Masking Description
Open Label
Allocation
Randomized
Enrollment
700 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
cpap group
Arm Type
Experimental
Arm Description
CPAP treatment plus conservative treatment with lifestyle modifications.
Arm Title
control group
Arm Type
Active Comparator
Arm Description
Conservative treatment with lifestyle modifications.
Intervention Type
Device
Intervention Name(s)
CPAP
Intervention Description
continuous positive pressure in the airway
Intervention Type
Other
Intervention Name(s)
conservative treatment
Intervention Description
conservative treatment group with lifestyle modifications
Primary Outcome Measure Information:
Title
To test whether treatment with CPAP in patients with moderate to severe OSAS and CKD in stages KDIGO G1-3, reduces the progression of renal disease (30% drop in GF) after 2 years of followed up.
Description
Number of participants with chronic kidney disease (CKD) and obstructive sleep apnea syndrome (OSAS) with a 30% decline in estimated glomerular filtration rate (eGFR) using the CKD-EPI (CKD Epidemiology Collaboration) 2009 creatinine equation after 2 years of followed up (each patient will be followed up for at least 2 years - range from 2 to 3 years)
Time Frame
after 2 years of followed up (each patient will be followed up for at least 2 years - range from 2 to 3 years)
Secondary Outcome Measure Information:
Title
To estimate the prevalence of OSAS in patients with CKD stages G1-3 KDIGO
Description
Number of participants with CKD and snoring and observed apneas with an apnea and hypoapnea index (AHI) ≥15/hour in home-based polysomnography.
Time Frame
after 2 years of followed up (each patient will be followed up for at least 2 years - range from 2 to 3 years)
Title
To test whether treatment with CPAP reduces the albumin / creatinine ratio in urine.
Description
Number of participants with CKD and OSAS with a decline in urine albumin to creatinine ratio.
Time Frame
after 2 years of followed up (each patient will be followed up for at least 2 years - range from 2 to 3 years)
Title
To evaluate whether treatment with CPAP reduces serum Cystatin C
Description
Number of participants with CKD and OSAS with a decline in serum cystatin C levels
Time Frame
after 2 years of followed up (each patient will be followed up for at least 2 years - range from 2 to 3 years)
Title
To evaluate whether treatment with CPAP reduces inflammation-endothelial disfunction markers
Description
Number of participants with CKD and OSAS with a decline in inflammation-endothelial disfunction markers (interleukine-6, interleukine-8, reactive C protein, sedimentation rate, asymmetric dimethylaginine or ADMA, intercellular adhesion molecule 1 or ICAM-1, vascular adhesion protein 1 or VCAM 1, vascular endothelial growth factor or VEGF)
Time Frame
after 2 years of followed up (each patient will be followed up for at least 2 years - range from 2 to 3 years)
Title
Evaluate whether treatment with CPAP reduces the progression of CKD to a different stage
Description
number of participants with CKD and OSAS with a change to a higher CKD stage according to eGFR.
Time Frame
after 2 years of followed up (each patient will be followed up for at least 2 years - range from 2 to 3 years)
Title
to test wheather CPAP reduces the percentage of patients achieving replacement therapy
Description
number of participants with CKD and OSAS who need renal replacement therapy (haemodialysis, peritoneal dialysis or renal transplantation)
Time Frame
after 2 years of followed up (each patient will be followed up for at least 2 years - range from 2 to 3 years)
Title
Evaluate wheather treatment with CPAP reduces the incidence of cardiovascular events
Description
number of participants with CKD and OSAS who suffered a cardiovascular event (myocardial infarction, stroke, hospitalization for heart failure, atrial fibrillation)
Time Frame
after 2 years of followed up (each patient will be followed up for at least 2 years - range from 2 to 3 years)
Title
Evaluate wheather treatment with CPAP reduces the mortality
Description
number of participants with CKD and OSAS with CPAP treatment who died (all-cause mortality)
Time Frame
after 2 years of followed up (each patient will be followed up for at least 2 years - range from 2 to 3 years)
Title
Evaluation of the cost-effectiveness of treatment groups with and without CPAP
Description
Cost-effectiveness of treatment groups conducting a cost-effectiveness study that allow us to estimate the incremental cost-effectiveness ratio (ICER) of CPAP treatment group compared to the conventional treatment group
Time Frame
after 2 years of followed up (each patient will be followed up for at least 2 years-range from 2 to 3 years)
Title
Compare the evolution of inflammation-endothelial disfunction markers in NO-OSAS group versus OSAS group
Description
Number of participants with NO-OSAS versus OSAS who have a decline in inflammation-endothelial disfunction markers (interleukine-6, interleukine-8, reactive C protein, sedimentation rate, asymmetric dimethylaginine or ADMA, intercellular adhesion molecule 1 or ICAM-1, vascular adhesion protein 1 or VCAM 1, vascular endothelial growth factor or VEGF)
Time Frame
after 2 years of followed up (each patient will be followed up for at least 2 years-range from 2 to 3 years)
Title
Compare the worsening of the glomerular filtration in NO OSAS group versus OSAS group
Description
number of participants with NO OSAS versus OSAS who have a worsening of the glomerular filtration.
Time Frame
after 2 years of followed up (each patient will be followed up for at least 2 years-range from 2 to 3 years)
Title
Compare the percentage of patients achieving renal replacement therapy in NO OSAS group versus OSAS group
Description
number of participants who need renal replacement therapy in NO OSAS group versus OSAS group
Time Frame
after 2 years of followed up (each patient will be followed up for at least 2 years-range from 2 to 3 years)
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Patients referred to the outpatient nephrology department with a diagnosis of chronic kidney disease stages G1-3 KDIGO
Older than18 years
Habitual snoring or observed apneas
Scale sleep sleepiness (Epworth Test) with 11 points or lower.
Exclusion Criteria:
Very debilitating chronic or neoplastic disease
Respiratory failure (PaO 2 <55 mm Hg).
Other symptoms of suspected sleep disorder different from OSAS.
Patients unable to perform self-administered questionnaires.
Patients with> 50% of central apnea or Cheyne-Stokes.
Patients who do not sign the informed consent.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Jaime Corral, MD
Phone
+34-927256204
Email
jcorral@separ.es
First Name & Middle Initial & Last Name or Official Title & Degree
Juan F Masa, PHD
Phone
+34-927256204
Email
fmasa@separ.es
Facility Information:
Facility Name
Jaime Corral
City
Cáceres
ZIP/Postal Code
10003
Country
Spain
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jaime Corral, MD
Phone
927256204
Email
jcorral@separ.es
12. IPD Sharing Statement
Plan to Share IPD
No
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Effect of CPAP in the Worsening of Renal Function in Early Stages of Chronic Kidney Disease (CKD)
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