End Stage Renal Disease Clinical Trial
Official title:
Effects of Hemodialysis on the Slee/Wake Cycle of Patients on Chronic Hemodialysis
The purpose of this study is to test a novel application of an existing treatment - using col dialysate (often used to treat hypotension) as opposed to warm dialysate (standard treatment) during hemodialysis for its ability to stabilize the sleep/wake cycle of patients receiving this chronic treatment
This competing continuation proposal follows NR04340, "The Effects of Hemodialysis on the
Sleep/ Wake Cycle", and seeks to test the efficacy of altering dialysate temperature on
nocturnal sleep and daytime sleepiness in patients on chronic hemodialysis (HD). During the
initial funding period, we examined the effects of HD and the time of its administration on
sleep and waking. The major findings were that, in comparison to a group of control subjects
with renal failure not yet on dialysis, HD subjects had reduced nocturnal total sleep time
and sleep efficiency and increased numbers of brief arousals. One-third of HD subjects had
abnormal, objectively measured daytime sleepiness, significant predictors of which were
indices of nocturnal sleep disorders and duration of HD treatment. These effects occurred
independent of treatment time of day. The negative influence of daytime sleepiness on life
quality and functioning that we also found highlights the importance of the development and
testing of interventions designed to address these changes. Furthermore, the recently
described relationship between sleep disorders/sleepiness and cardiovascular disease leading
cause of death in HD patients underscores the importance of this work.
Within the context of the Two-Process Model of Sleep Regulation and the well-described
relationship between sleep/wake state and body temperature (BT), the data from additional
studies we have conducted indicate that HD associated heat production contributes to its
iatrogenic effects on the sleep/wake cycle. Consistent with other reports, we have shown
that HD causes an increase in BT and, furthermore, alters its course across the day. We have
also shown that BT and state sleepiness predictably covary across the duration of HD and
that HD is associated with increased levels of both subjective and objective measurements of
sleepiness. From both theoretical and physiological perspectives, one would predict that
these HD-induced changes would place patients at high-risk for sleep/wake disturbances. In
fact, both the nocturnal and daytime polysomnographic studies we conducted during our
initial funding period demonstrate the severity of the sleep/wake problems experienced by
this group. Previously tested interventions designed to improve the sleep of HD patients,
such as normalizing hematocrit and performing slow, nocturnal HD, have decreased periodic
limb movements and sleep apnea respectively, but have failed to significantly improve other
indices of nocturnal sleep quality. We thus conducted a pilot study to test our hypothesis
that treatment induced changes in BT contribute to the fragmented nocturnal sleep seen in
this group by using cool dialysate (an existing intervention used to reduce hypotension) to
block heat production and stabilize the sleep/wake cycle. Preliminary results demonstrated
that, after one treatment, this intervention markedly normalized the rhythm of BT and
improved indices of nocturnal sleep quantity and quality. Therefore, a major component of
this proposal is to test a novel application for a safe, non-pharmacologic, cost-effective
intervention that is already in use in clinical practice - using cool dialysate during HD to
help stabilize the sleep/wake cycle of chronic HD patients. We will also evaluate its
effects on selected sleep-related physiologic, psychological, behavioral, and general health
outcomes.
This study, a randomized, single-blinded, control group clinical trial, represents the
logical progression of a program of research devoted to the development of interventions
designed to optimize the sleep/wake patterns of patients on chronic HD. The specific aims
and associated hypotheses are:
1. To test the effects of using cool dialysate during HD in comparison to warm dialysate
(standard treatment) on the sleep/wake cycle of patients with chronic renal failure.
H1 HD subjects will have improved nocturnal sleep (objective and subjective measures of
sleep latency, total sleep time, sleep efficiency, and sleep disturbance) when dialyzed
with cool dialysate in comparison to a warm dialysate.
H2 HD subjects will have decreased daytime sleepiness (physiologic, manifest, and
introspective) when dialyzed with cool dialysate in comparison to warm dialysate .
2. To test the effects of using cool dialysate during HD in comparison to warm dialysate
on other sleep-related physiological, psychological, behavioral, and general health
outcomes.
H3 HD subjects will demonstrate improvement in selected sleep-related physiological
(distal/proximal skin gradient and axillary body temperature rhythm), psychological (mood),
behavioral (daily rest/activity), and general health outcomes (quality of life and
functional status) when dialyzed with cool dialysate in comparison to warm dialysate.
;
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Treatment
| Status | Clinical Trial | Phase | |
|---|---|---|---|
| Completed |
NCT04076488 -
Feasibility of an Interactive Tablet-based Exercise Program for People With Chronical Diseases
|
N/A | |
| Completed |
NCT03289650 -
Extended Release Tacrolimus vs. Twice-Daily Tacrolimus
|
Phase 3 | |
| Completed |
NCT04042324 -
A Study to Investigate the Effect of Triferic Plus Heparin Infusion Compared to Heparin Alone on Coagulation Parameters in Hemodialysis Patients
|
Phase 1/Phase 2 | |
| Completed |
NCT01242904 -
Use of a Bimodal Solution for Peritoneal Dialysis
|
Phase 2 | |
| Active, not recruiting |
NCT03183245 -
Comparison of the Human Acellular Vessel (HAV) With Fistulas as Conduits for Hemodialysis
|
Phase 3 | |
| Completed |
NCT03257410 -
Theranova 400 Dialyzer In End Stage Renal Disease (ESRD) Patients
|
N/A | |
| Completed |
NCT03627299 -
Renal Transplants in Hepatitis C Negative Recipients With Nucleic Acid Positive Donors
|
Phase 4 | |
| Recruiting |
NCT05917795 -
Endoscopic Sleeve Gastroplasty With Endomina® for the Treatment of Obesity in Kidney Transplant Candidates
|
N/A | |
| Terminated |
NCT03539861 -
Immunomodulatory Biomimetic Device to Treat Myocardial Stunning in End-stage Renal Disease Patients
|
N/A | |
| Withdrawn |
NCT02130817 -
Belatacept in Kidney Transplantation of Moderately Sensitized Patients
|
Phase 4 | |
| Completed |
NCT05540457 -
Evaluation of Non-Invasive Continuous vs Intermittent BloodPressure Monitors in Maintenance Dialysis (BP Dialysis)
|
N/A | |
| Not yet recruiting |
NCT04900610 -
The Effect of Vitamin K2 Supplementation on Arterial Stifness and Cardiovascular Events in PEritonial DIAlysis
|
N/A | |
| Recruiting |
NCT02176434 -
Pilot Feasibility Study of Combined Kidney and Hematopoietic Stem Cell Transplantation to Cure End-stage Renal Disease
|
N/A | |
| Active, not recruiting |
NCT02581449 -
Effect of Omega-3 Fatty Acids on Oxidative Stress and Dyslipidemia in Pediatric Patients Undergoing Hemodialysis
|
Phase 2 | |
| Completed |
NCT02832466 -
Quantifying the Deterioration of Physical Function in Renal Patients
|
N/A | |
| Completed |
NCT02134314 -
C1INH Inhibitor Preoperative and Post Kidney Transplant to Prevent DGF & IRI
|
Phase 1/Phase 2 | |
| Completed |
NCT02215655 -
Increasing Autonomous Motivation in ESRD to Enhance Phosphate Binder Adherence
|
N/A | |
| Completed |
NCT02830490 -
Reliability of Functional Measures in Hemodialysis Patient.
|
N/A | |
| Completed |
NCT02832440 -
Comparison of Two Exercise Programmes in Patients Undergoing Hemodialysis
|
N/A | |
| Recruiting |
NCT01912001 -
Virtual Ward for Home Dialysis
|
N/A |