Furosemide Alone or Unexpectedly With Solution of Hypertonic Saline in Nephrotic Syndrome (FLUSH-NS)
Primary Purpose
Nephrotic Syndrome
Status
Recruiting
Phase
Not Applicable
Locations
Poland
Study Type
Interventional
Intervention
Hypertonic saline
Furosemide Injection
Sponsored by
About this trial
This is an interventional treatment trial for Nephrotic Syndrome focused on measuring diuretics
Eligibility Criteria
Inclusion Criteria:
- 30 consecutive patients with nephrotic syndrome (proteinuria over 3.5 g/day, edema, hypoalbuminemia, dysproteinemia) admitted to II Nephrology Department from November 2018 onwards within 48h of admission,
- age above 18,
- informed consent.
Exclusion Criteria:
- AKI (acute kidney injury) - AKIN criteria level 3,
- CKD (chronic kidney disease) stage 4 and 5 according to KDIGO (Kidney Disease: Improving Global Outcomes),
- concomittant heart failure NYHA (New York Heart Association) class III or worse,
- active liver disease and liver failure,
- terminal neoplastic disease,
- serum sodium above 145 mmol/l,
- pregnancy.
Sites / Locations
- II Department of Nephrology and HypertensionRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
high-dose furosemide & hypertonic saline
high-dose furosemide
Arm Description
furosemide i.v., 3% NaCl
furosemide i.v.
Outcomes
Primary Outcome Measures
Diuresis
ml of diuresis
Secondary Outcome Measures
Length of hospitalisation
days
BNP levels
pg/ml
Full Information
NCT ID
NCT03750136
First Posted
November 20, 2018
Last Updated
November 19, 2022
Sponsor
Medical University of Bialystok
1. Study Identification
Unique Protocol Identification Number
NCT03750136
Brief Title
Furosemide Alone or Unexpectedly With Solution of Hypertonic Saline in Nephrotic Syndrome
Acronym
FLUSH-NS
Official Title
HSS (Hypertonic Saline Solution) Plus High Dose Furosemide vs High Dose Furosemide in Nephrotic Syndrome - a Randomized Trial
Study Type
Interventional
2. Study Status
Record Verification Date
November 2022
Overall Recruitment Status
Recruiting
Study Start Date
December 15, 2018 (Actual)
Primary Completion Date
January 1, 2023 (Anticipated)
Study Completion Date
March 1, 2023 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Medical University of Bialystok
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
The trial will test the hypothesis that hypertonic saline on top of standard diuretic treatment will help achieve adequate diuresis in patients with nephrotic syndrome.
Detailed Description
Objectives:
Edema is one of the major clinical manifestations of nephrotic syndrome. All patients are initially treated with diuretics and sodium restriction but the results are sometimes not satisfactory. Hypertonic saline solutions have been studied in congestive heart failure and a meta-analysis confirmed it's role in achieving adequate diuresis and protecting patients against acute kidney injury although the proposed mechanism of action is not known (osmotic action?, inhibition of renin-angiotensin-aldostrerone system?, increase in renal perfusion?, myocardial contractility?). The investigators therefore hypothesized that it may exert beneficial effects also in nephrotic syndrome.
Treatment protocol:
A prospective placebo-controlled randomized trial. Subjects will be randomized to high-dose furosemide vs high-dose furosemide plus hypertonic intravenous saline in a 1:1 fashion. All subjects will receive furosemide tid (starting with 3x40 mg i.v.) with or without hypertonic saline solution (3x100 ml of 3% NaCl - in a combined infusion lasting 10 minutes). Subjects randomized to furosemide only will receive 3x100 ml of 5% glucose (in a combined infusion lasting 10 minutes). The dose of furosemide will be determined by the investigator based on patients weight, severity of edema, 24-h urine volume, kidney function. In case of poor clinical response (urine volume below 1000 ml) the investigator will be able to titrate the furosemide dose up to 3x180 mg i.v. All patients will be kept on low-salt diet and water restriction (500-1000 ml/day), their weight will assessed every morning before breakfast and measurement of 24-h urine volume will be performed every day. Additionally BNP levels will be measured at baseline and after 5 days of treatment. Treatment will be continued for 5 days. The primary measure of efficacy will be urine volume and the rate of acute kidney injury (AKI), secondary measure of efficacy will be the expected decrease in brain natriuretic peptides (BNP) levels and the length of hospitalization.
Hydrochlorothiazide, spironolactone and other diuretics use will be contraindicated during the study. Patients will be required to receive standard concurrent therapy as determined by their attending physician and according to current guidelines (including steroids and other immunosuppresives).
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Nephrotic Syndrome
Keywords
diuretics
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Investigator
Allocation
Randomized
Enrollment
30 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
high-dose furosemide & hypertonic saline
Arm Type
Experimental
Arm Description
furosemide i.v., 3% NaCl
Arm Title
high-dose furosemide
Arm Type
Active Comparator
Arm Description
furosemide i.v.
Intervention Type
Drug
Intervention Name(s)
Hypertonic saline
Other Intervention Name(s)
3% saline
Intervention Description
high dose furosemide with hypertonic saline 3x daily
Intervention Type
Drug
Intervention Name(s)
Furosemide Injection
Intervention Description
high dose furosemide
Primary Outcome Measure Information:
Title
Diuresis
Description
ml of diuresis
Time Frame
5 days
Secondary Outcome Measure Information:
Title
Length of hospitalisation
Description
days
Time Frame
14 days
Title
BNP levels
Description
pg/ml
Time Frame
5 days
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
30 consecutive patients with nephrotic syndrome (proteinuria over 3.5 g/day, edema, hypoalbuminemia, dysproteinemia) admitted to II Nephrology Department from November 2018 onwards within 48h of admission,
age above 18,
informed consent.
Exclusion Criteria:
AKI (acute kidney injury) - AKIN criteria level 3,
CKD (chronic kidney disease) stage 4 and 5 according to KDIGO (Kidney Disease: Improving Global Outcomes),
concomittant heart failure NYHA (New York Heart Association) class III or worse,
active liver disease and liver failure,
terminal neoplastic disease,
serum sodium above 145 mmol/l,
pregnancy.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Alicja Rydzewska-Rosolowska, MD
Phone
+48858317885
Email
alicja.rosolowska@umb.edu.pl
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Alicja Rydzewska-Rosolowska, MD
Organizational Affiliation
Medical University of Białystok
Official's Role
Principal Investigator
Facility Information:
Facility Name
II Department of Nephrology and Hypertension
City
Bialystok
ZIP/Postal Code
15-276
Country
Poland
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Alicja Rydzewska-Rosolowska, MD
Phone
+48858317885
Email
alicja.rosolowska@umb.edu.pl
12. IPD Sharing Statement
Plan to Share IPD
Yes
Citations:
PubMed Identifier
12660669
Citation
Licata G, Di Pasquale P, Parrinello G, Cardinale A, Scandurra A, Follone G, Argano C, Tuttolomondo A, Paterna S. Effects of high-dose furosemide and small-volume hypertonic saline solution infusion in comparison with a high dose of furosemide as bolus in refractory congestive heart failure: long-term effects. Am Heart J. 2003 Mar;145(3):459-66. doi: 10.1067/mhj.2003.166.
Results Reference
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PubMed Identifier
10915397
Citation
Paterna S, Parrinello G, Amato P, Dominguez L, Pinto A, Maniscalchi T, Cardinale A, Licata A, Amato V, Licata G, Di Pasquale P. Tolerability and efficacy of high-dose furosemide and small-volume hypertonic saline solution in refractory congestive heart failure. Adv Ther. 1999 Sep-Oct;16(5):219-28.
Results Reference
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PubMed Identifier
10938493
Citation
Paterna S, Di Pasquale P, Parrinello G, Amato P, Cardinale A, Follone G, Giubilato A, Licata G. Effects of high-dose furosemide and small-volume hypertonic saline solution infusion in comparison with a high dose of furosemide as a bolus, in refractory congestive heart failure. Eur J Heart Fail. 2000 Sep;2(3):305-13. doi: 10.1016/s1388-9842(00)00094-5.
Results Reference
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Furosemide Alone or Unexpectedly With Solution of Hypertonic Saline in Nephrotic Syndrome
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