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Not listed Not applicable Interventional

Assisted Peritoneal Dialysis: A Feasibility Study

ClinicalTrials.gov ID: NCT04319185

Public ClinicalTrials.gov record NCT04319185. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 10, 2026, 9:38 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

Patients with End-Stage Kidney Disease (ESKD) wishing to choose Peritoneal Dialysis (PD) may not be able to perform this modality due to advanced age, physical function/dexterity, vision, cognition, mobility, or psychosocial issues. This intervention will seek to test the feasibility of a clinical support model to address these barriers. Patients identified by their nephrologist as wishing to choose Peritoneal Dialysis (PD), but needing assistance, are referred to the research staff for discussion and consent. Based on the assessment of the subject's nephrologist, PD staff, and researchers, the subject will receive assistance beyond the standard PD care offered in US dialysis centers. Such assistance will be provided for up to one visit/day, seven days/week, for up to three months. At the end of that time period, the subject will be able to perform PD independently, have identified a care provider, or have planned with his/her nephrologist for an alternative dialysis modality.

Study identification

NCT ID
NCT04319185
Recruitment status
Not listed
Study type
Interventional
Phase
Not applicable
Lead sponsor
Satellite Healthcare
Other
Enrollment
20 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Sep 10, 2020
Primary completion
Nov 29, 2021
Completion
Dec 30, 2021
Last update posted
Sep 21, 2021

2020 – 2021

United States locations

U.S. sites
6
U.S. states
1
U.S. cities
6
Facility City State ZIP Site status
Satellite WellBound Emeryville Emeryville California 94608 Recruiting
Satellite WellBound Fremont Fremont California 94538 Recruiting
Satellite WellBound Milpitas Milpitas California 95035 Recruiting
Satellite WellBound Mountain View Mountain View California 94040 Recruiting
Satellite WellBound San Jose San Jose California 95125 Recruiting
Satellite WellBound San Mateo San Mateo California 94403 Recruiting

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT04319185, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Sep 21, 2021 · Synced Sep 10, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT04319185 live on ClinicalTrials.gov.

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