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NCT03827720 · ClinicalTrials.gov registry record · NA

Early Feasibility Study of the SENSE Device

A NA study, sponsored by Sense Diagnostics.

Completed
Registry status
NA
Development phase
20
Enrollment target

NCT03827720: Completed NA study, sponsored by Sense Diagnostics.

NCT03827720 is a NA study that has completed, run by Sense Diagnostics. The registered enrollment target is 20 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (99% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT03827720, a NA study, has completed, sponsored by Sense Diagnostics.

COMPLETED
Registry status
NA
Development phase
20 participants
Enrollment target

Study Summary

A single site, study of the SENSE device in up to 20 study subjects, (five healthy controls and five each with ICH, AIS with LVO and AIS without LVO) in whom SENSE can be applied within 24 hours of stroke symptom onset.

Primary Outcome

The change in received power (PR) measured by the SENSE device will be calculated and the accuracy of the SENSE algorithm will be tested for the SENSE measurement that correspond with diagnostic CT scan for stroke severity, hemorrhage volume and in the case of AIS, presence or absence of LVO..

Interventions

  • DEVICE SENSE Device

Trial Details

FieldValue
Enrollment Target 20 participants
Start Date 2019-06-06
Est. Completion 2021-01-04
Phase NA
Sense Diagnostics

4 total trials

What the finished NCT03827720 record still lists

NCT03827720 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 20 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (99% lower).

The record links to 0 conditions, and to 1 intervention - of which SENSE Device is the first listed.

NCT03827720 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT03827720 about?

NCT03827720 is a clinical study titled "Early Feasibility Study of the SENSE Device". A single site, study of the SENSE device in up to 20 study subjects, (five healthy controls and five each with ICH, AIS with LVO and AIS without LVO) in whom SENSE can be applied within 24 hours of stroke symptom onset.

What is the current status of trial NCT03827720?

This trial is currently completed. It is a NA study. The enrollment target is 20 participants. The study started on 2019-06-06. Estimated completion is 2021-01-04.

What interventions are being tested in trial NCT03827720?

The interventions under investigation include: SENSE Device (DEVICE).

Who is sponsoring clinical trial NCT03827720?

This trial is sponsored by Sense Diagnostics, which has 4 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT03827720's enrollment target sits among peer trials

20 1768th of 2000 higher than 140 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 NCT03827720, the US trial registry maintained by the National Library of Medicine. NCT03827720 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.