Reducing Arrhythmia in Dialysis by Adjusting the Rx Electrolytes/Ultrafiltration, Study B

End Stage Renal Disease Clinical Trial

— RADAR-B  

Official title:

RADAR-B: A Phase 2 Multi-center Study to Evaluate the Safety and Tolerability of Using Point-of-Care-Guided Manipulation of Ultrafiltration Rate to Prevent Hemodialysis-Associated Arrhythmias

Clinical Trial Details — Status: Withdrawn

Administrative data

• NCT number: NCT03519360
• Other study ID #: 2017P001737-
• Secondary ID: R34HL140477-01
• Status: Withdrawn
• Phase: N/A
• Start date: July 1, 2019
• Est. completion date: February 1, 2021

Study information

• Verified date: July 2021
• Source: NYU Langone Health
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The purpose of this study is to test the feasibility of trials that change the dialysis ultrafiltration rate (UFR) by limiting the maximum rate and to estimate the extent to which limiting the ultrafiltration rate reduces the risk of abnormal heart rhythms in people with kidney failure who are being treated with chronic hemodialysis.

Description:

Within four weeks of consent, subjects will have an Implantable Loop Recorder (ILR) (Medtronic LINQ) device implanted. Subjects will be given a transmitter/charger and a Patient Care Assistant which they will be required to keep for the duration of their participation in the study. ILR tracings will be uploaded automatically and reviewed by the study team for the occurrence of clinically significant arrhythmia.

Following ILR implantation, subjects will alternate between weekly periods in which the ultrafiltration rate can be unlimited or in which the ultrafiltration rate is limited to ≤10mL/kg/hour.

Recruitment information / eligibility

• Status: Withdrawn
• Enrollment: 0
• Est. completion date: February 1, 2021
• Est. primary completion date: February 1, 2021
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 85 Years

Eligibility

Inclusion Criteria:

• Maintenance hemodialysis therapy for end-stage renal disease

• Age 18-85 years (subjects between 18-40 years old will be required to have at least one of the following: history of congestive failure, diabetes, coronary or peripheral vascular disease, or arrhythmia)

• >30 days since dialysis initiation

• Ability to provide informed consent

• Interdialytic weight gain necessitating an UF rate of =13mL/kg/hour of dialysis to achieve the target post-dialysis weight in at least half of the dialysis sessions (=6 sessions) in the month prior to enrollment

Exclusion Criteria:

• Expected survival <6 months-to allow trial completion

• Renal transplant, transfer to home or peritoneal dialysis, or to non-study hemodialysis facility anticipated within 6 months

• Prisoners or cognitive disability preventing informed consent

• Pregnancy. A pregnancy test will be required for women of child bearing potential prior to enrollment. A pregnancy test will not be required for women past the age of child-bearing potential >55 years old, women with a history of surgical sterilization, or for women <55 years of age who have not had a menses within the past 12 months

• Skin condition, immune dysfunction, history of multiple infections or other condition which increases risk of local infection with ILR placement

• Bleeding disorder or anti-coagulation that cannot be reversed for ILR placement

• Existing pacemaker, implantable monitor or defibrillator which precludes device placement

• Chronic, persistent AF (defined as the presence of persistent AF on all available EKGs at time of recent screening)

Related Conditions & MeSH terms

• Arrhythmias, Cardiac
• End Stage Renal Disease
• Kidney Failure, Chronic

Intervention

Other:
• UFR-restricted dialysis
UFR's are limited to a maximum of 10 mL/kg/hr for the duration of the session. In order to prevent progressive volume overload and the need for additional hemodialysis sessions to manage volume gains in this scenario, subjects will crossover weekly between the restricted and unrestricted UFR interventions.
• UFR-unrestricted dialysis
UFR's will be unlimited and prescribed according to the standard of care.

Locations

Country	Name	City	State
United States	Duke University Medical Center	Durham	North Carolina

Sponsors (4)

Lead Sponsor	Collaborator
NYU Langone Health	Duke University, National Heart, Lung, and Blood Institute (NHLBI), National Institutes of Health (NIH)

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Other	Identification of barriers to implementation	HD staff and patients will be surveyed once 3 subjects have completed 1 month of each trial and once 6 patients have completed each trial to identify barriers to implementation of the protocol.	2 years
Other	Association of dialysis day, shift, and site with CSA	Exploratory analyses will assess association of dialysis day (Monday/Wednesday/Friday or Tuesday/Thursday/Saturday), shift (1st-3rd), and site with CSA.	2 years
Other	Association of dialysis day, shift, and site with adherence	Exploratory analyses will assess association of dialysis day (Monday/Wednesday/Friday or Tuesday/Thursday/Saturday), shift (1st-3rd), and site with adherence.	2 years
Other	Association of demographic and pre-randomization factors with adverse events	Exploratory analyses will assess age, sex, race, mean intra-dialytic weight gain, and mean UFR in month prior to randomization on the incidence of adverse events.	2 years
Primary	Adherence with Proposed Interventions	Adherence will be assessed as the percent of sessions in which the mandated UFR is delivered.	2 years
Primary	Incidence of unscheduled hemodialysis or hospitalization for volume overload	The occurrence of unscheduled hemodialysis or ultrafiltration sessions needed to treat volume overload will be measured to assess the impact of the UFR intervention on the adequacy of volume removal.	4 months
Primary	Change in duration of clinically significant arrhythmia (CSA) per month	The total monthly duration of CSA (in minutes) will be utilized as the primary efficacy endpoint in comparing this pair of interventions (aggressive vs. conservative UF). In the event of incomplete follow-up, CSA duration will be indexed to follow-up time. CSA will be defined on the basis of arrhythmias likely to lead to sudden cardiac arrest (SCA) or serious morbidity and mortality and will include AF, asystole =3 seconds, bradycardia =40 beats per minute lasting =6 seconds, and sustained VT =130 beats per minute lasting =30 seconds. CSA's will be adjudicated by study electrophysiologists.	4 months
Secondary	Comparison of pre- and post-correction adherence	This measure will assess adherence to the protocol following any corrective measures made in response to surveys of dialysis staff.	2 years
Secondary	Association of individual interventions with atrial fibrillation (AF)	This measure will assess the effect of the interventions on the duration of atrial fibrillation.	4 months
Secondary	Association of individual interventions on potentially lethal arrhythmia	This measure will assess the effect of the interventions on the duration of potentially lethal arrhythmias defined as asystole, sustained VT, bradycardia for =6 seconds.	4 months
Secondary	The occurrence of clinically significant arrhythmias requiring intervention	This measure will assess the effect of the interventions on occurrence of arrhythmia requiring clinical intervention.	4 months
Secondary	All-cause mortality	This measure will assess the effect of the interventions on occurrence of all-cause mortality.	2 years
Secondary	Cardiovascular mortality	This measure will assess the effect of the interventions on occurrence of cardiovascular mortality.	2 years
Secondary	Hospitalization	This measure will assess the effect of the interventions on occurrence of hospitalizations.	2 years
Secondary	Proportion of screened patients enrolled	The percent of screened patients enrolled will be calculated as a secondary feasibility measure to assess the size of the necessary screening pool. Reasons for non-enrollment (vis-à-vis inclusion and exclusion criteria and patient and physician preferences) will be assessed to determine the potential for protocol modification to improve recruitment.	2 years