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Directed Use of REmote Patient Management System AMia to Achieve Prescribed Dry Weight
NCT04002440 · View on ClinicalTrials.gov ↗
Study Summary
Among ambulatory peritoneal dialysis patients, does use of the Baxter AMIA peritoneal dialysis cycler with SHARESOURCE connectivity platform achieve dry weight targets better than use of the Baxter Home Choice Pro cycler.
Conditions Studied
Interventions
- COMBINATION_PRODUCT AMIA with SHARESOURCE Connectivity Platform
- DEVICE HomeChoice PRO
Study Locations (2)
California
- Home Dialysis Therapies of San Diego — Chula Vista
- Home Dialysis Therapies of San Diego — San Diego
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 28 participants |
| Start Date | 2018-11-08 |
| Est. Completion | 2022-04 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT04002440
The ClinicalTrials.gov registry entry for NCT04002440 describes a study currently listed as active not recruiting. It is categorized as NA, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 28 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of California, San Diego, which has 823 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 2 conditions, with Safety Issues appearing as the primary indexed condition, and to 2 interventions — of which AMIA with SHARESOURCE Connectivity Platform is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.
Geographic footprint matters for practical reasons: NCT04002440 reports 2 study locations spanning 1 distinct geographic area — top geographies include California. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.
Frequently Asked Questions
What is clinical trial NCT04002440 about?
NCT04002440 is a clinical study titled "Directed Use of REmote Patient Management System AMia to Achieve Prescribed Dry Weight". Among ambulatory peritoneal dialysis patients, does use of the Baxter AMIA peritoneal dialysis cycler with SHARESOURCE connectivity platform achieve dry weight targets better than use of the Baxter Home Choice Pro cycler.
What is the current status of trial NCT04002440?
This trial is currently active not recruiting. It is a NA study. The enrollment target is 28 participants. The study started on 2018-11-08. Estimated completion is 2022-04.
What conditions does trial NCT04002440 study?
This clinical trial studies the following conditions: Safety Issues, Efficacy. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT04002440?
The interventions under investigation include: AMIA with SHARESOURCE Connectivity Platform (COMBINATION_PRODUCT), HomeChoice PRO (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT04002440?
This trial is sponsored by University of California, San Diego, which has 823 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT04002440 being conducted?
This trial has 2 study locations across California. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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