Clinical Trials Directory

Trials / Terminated

TerminatedNCT02975505

Pilot to Examine Risk and Feasibility of Remote Management of BP From CKD Through ESRD

Status
Terminated
Phase
N/A
Study type
Interventional
Enrollment
108 (actual)
Sponsor
University of California, San Francisco · Academic / Other
Sex
All
Age
16 Years
Healthy volunteers
Not accepted

Summary

The transition from chronic kidney disease (CKD) to end-stage renal disease ESRD is a vulnerable and challenging period of time for patients and providers. Suboptimal control of blood pressure is known to be common in patients with the advanced stages of CKD, and may contribute to their elevated risk of progression to ESRD, cardiovascular morbidity, and mortality. This proposal is a pilot randomized controlled trial designed to test whether intensive home blood pressure lowering is feasible and safe in patients with advanced CKD as they transition to ESRD.

Detailed description

The transition from advanced chronic kidney disease (CKD), when estimated glomerular filtration rate (eGFR) is \<=30 mL/min/1.73m2, to end-stage renal disease (ESRD) represents a vulnerable period, when multiple physiologic and psychosocial changes occur as patients prepare for either dialysis or kidney transplant. This study is a pilot randomized controlled trial to test the safety and feasibility of studying strict versus usual BP control in a population of patients with advanced CKD (eGFR \<=30 mL/min/1.73m2), including those with diabetes. For this pilot study, we will randomize 120 patients with advanced CKD who have elevated BP to either a home SBP target of \<120 mm Hg (intervention group) versus usual care (130-140 mmHg).

Conditions

Interventions

TypeNameDescription
OTHERStrict blood pressure controlSystolic Blood Pressure Target \< 120 mm Hg (measured at home)

Timeline

Start date
2017-02-10
Primary completion
2021-07-18
Completion
2021-07-18
First posted
2016-11-29
Last updated
2025-02-17
Results posted
2025-02-17

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT02975505. Inclusion in this directory is not an endorsement.