This study is not yet accepting patients

Outpatient Recovery From Acute Kidney Injury Requiring Dialysis - 2

a study on Acute Kidney Injury Dialysis

Summary

Eligibility
for people ages 18 years and up (full criteria)
Location
at San Francisco, California
Dates
study started
study ends around
Principal Investigator
by Ian E McCoy, MD, MS
Headshot of Ian E McCoy
Ian E McCoy

Description

Summary

Providing additional information to patients with acute kidney injury who continue dialysis after hospital discharge and to the accepting kidney doctor (nephrologist) who manages their dialysis may be feasible and beneficial. This study will pilot measuring the patient's residual kidney function at the time of discharge and communicating that result to the accepting nephrologist and the patient, along with information on recommended recovery monitoring frequency and criteria for consideration of a twice-weekly hemodialysis schedule.

Keywords

AKI, AKI - Acute Kidney Injury, Dialysis Patients, Acute Kidney Injury, Wounds and Injuries, Transmission of additional AKI-D recovery information, No additional AKI-D recovery information, Additional AKI-D recovery information

Eligibility

You can join if…

Open to people ages 18 years and up

  • AKI-D (not ESKD, as determined by the clinical inpatient nephrology team)
  • Age ≥ 18 years
  • Planned for continued dialysis outside the acute hospital setting (at outpatient dialysis unit/SNF/LTACH, not planned transfer to another short-stay acute care hospital).

You CAN'T join if...

  • Pregnant
  • Prisoner
  • Unable to consent and no surrogate decision maker available
  • Clinical team declines to allow approach for study

Location

  • UCSF
    San Francisco California 94143 United States

Lead Scientist at UCSF

  • Ian E McCoy, MD, MS
    Dr. McCoy is a nephrologist and clinical researcher. His research focuses acute kidney injury, particularly dialysis-requiring acute kidney injury.

Details

Status
not yet accepting patients
Start Date
Completion Date
(estimated)
Sponsor
University of California, San Francisco
ID
NCT07106151
Study Type
Interventional
Participants
Expecting 40 study participants
Last Updated