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NCT04087213 · ClinicalTrials.gov registry record · NA

Study of HemoCare™ Hemodialysis System for Home Nocturnal Dialysis in Patients With ESRD

A NA study, sponsored by Deka Research and Development.

Completed
Registry status
NA
Development phase
36
Enrollment target

NCT04087213: Completed NA study, sponsored by Deka Research and Development.

NCT04087213 is a NA study that has completed, run by Deka Research and Development. The registered enrollment target is 36 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (97% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT04087213, a NA study, has completed, sponsored by Deka Research and Development.

COMPLETED
Registry status
NA
Development phase
36 participants
Enrollment target

Study Summary

This prospective multi-center, open-label, single-arm study intends to gather and evaluate safety data for the nocturnal use of the HemoCare™ Hemodialysis System.

Primary Outcome

Adverse event (AE) rate per 100 HemoCare™ Hemodialysis System treatments during Assisted and Unassisted Home Evaluable Periods

Interventions

  • DEVICE HemoCare™ Hemodialysis System

Trial Details

FieldValue
Enrollment Target 36 participants
Start Date 2019-09-05
Est. Completion 2023-01-11
Phase NA
Deka Research and Development

4 total trials

What the finished NCT04087213 record still lists

NCT04087213 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 36 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (97% lower).

The record links to 0 conditions, and to 1 intervention - of which HemoCare™ Hemodialysis System is the first listed.

NCT04087213 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT04087213 about?

NCT04087213 is a clinical study titled "Study of HemoCare™ Hemodialysis System for Home Nocturnal Dialysis in Patients With ESRD". This prospective multi-center, open-label, single-arm study intends to gather and evaluate safety data for the nocturnal use of the HemoCare™ Hemodialysis System.

What is the current status of trial NCT04087213?

This trial is currently completed. It is a NA study. The enrollment target is 36 participants. The study started on 2019-09-05. Estimated completion is 2023-01-11.

What interventions are being tested in trial NCT04087213?

The interventions under investigation include: HemoCare™ Hemodialysis System (DEVICE).

Who is sponsoring clinical trial NCT04087213?

This trial is sponsored by Deka Research and Development, which has 4 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT04087213's enrollment target sits among peer trials

36 1541st of 2000 higher than 437 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT04087213, the US trial registry maintained by the National Library of Medicine. NCT04087213 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.