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Using Continuous Positive Airway Pressure to Reduce the Incidence of Acute Kidney Injury in Hospitalized Patients With Chronic Kidney Disease

University of South Florida logo

University of South Florida

Status

Withdrawn

Conditions

Chronic Kidney Disease
Obstructive Sleep Apnea

Treatments

Device: CPAP/autopap

Study type

Interventional

Funder types

Other

Identifiers

NCT01859260
TGHCPAPCKD

Details and patient eligibility

About

Obstructive sleep apnea (OSA) is a common and undertreated condition in patients with chronic kidney disease (CKD). Both physiologic and empiric data suggest that renal hypoxia due to OSA is associated with worsening kidney function. Hospitalized patients are often exposed to multiple nephrotoxins such as antibiotics, contrast agents, and diuretics, which place them at risk for acute worsening of kidney function. This study aims to determine whether immediate diagnosis and treatment of OSA in CKD patients will decrease the incidence of acute kidney injury during hospitalization. The investigators will evaluate the extent to which this effect can be attributed to a decrease in nocturnal hypoxia and improved blood pressure control. Secondary endpoints include hospital length of stay, and a composite outcome comprised of hemodialysis initiation, major cardiovascular events, and mortality.

Sex

All

Ages

19+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. CKD defined by National Kidney Foundation Staging system: eGFR < 60
  2. Overnight sleep study consistent with OSA

Exclusion criteria

  1. Currently treated with positive airway pressure for sleep-disordered breathing
  2. Hemodynamically unstable, defined as SBP < 90, or use of vasopressors
  3. Intubated or mechanically ventilated
  4. Respiratory insufficiency, defined as P/F ratio < 250, or requiring mechanical ventilation
  5. End stage renal disease on renal replacement therapy
  6. Contraindication to CPAP, including active emesis, recent intracranial surgery, altered level of consciousness

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

0 participants in 2 patient groups

Control
No Intervention group
Intervention
Experimental group
Description:
CPAP/autopap
Treatment:
Device: CPAP/autopap

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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