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NCT06442358 · ClinicalTrials.gov registry record · NA

Self Biophysical Profile Using a Home Ultrasound Device Proof of Concept

A NA study of Perinatal Care, sponsored by PulseNmore.

Completed
Registry status
NA
Development phase
25
Enrollment target
1
Study location

NCT06442358: Completed NA study of Perinatal Care, sponsored by PulseNmore.

NCT06442358 is a NA study of Perinatal Care that has completed, run by PulseNmore. The registered enrollment target is 25 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (98% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT06442358, a NA study of Perinatal Care, has completed, sponsored by PulseNmore.

COMPLETED
Registry status
NA
Development phase
25 participants
Enrollment target
1
Study location

Study Summary

The objective of this study is to assess if patients presenting for antenatal testing can complete a Bio Physical Score (BPP) with a home-use ultrasound with remote clinician guidance.

Primary Outcome

Assessment will done by determining fetal movement, fetal tone, fetal breathing, and amniotic fluid level

Conditions Studied

Interventions

  • DEVICE Pulsenmore ES home ultrasound device

Study Locations (1)

Michigan

  • University of Michigan - Ann Arbor

Trial Details

FieldValue
Enrollment Target 25 participants
Start Date 2024-04-10
Est. Completion 2024-12-30
Phase NA
PulseNmore

3 total trials

What the finished NCT06442358 record still lists

NCT06442358 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 25 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (98% lower).

The record links to 1 condition, with Perinatal Care appearing as the primary indexed condition, and to 1 intervention - of which Pulsenmore ES home ultrasound device is the first listed.

NCT06442358 reports a single indexed study location in Michigan.

Frequently Asked Questions

What is clinical trial NCT06442358 about?

NCT06442358 is a clinical study titled "Self Biophysical Profile Using a Home Ultrasound Device Proof of Concept". The objective of this study is to assess if patients presenting for antenatal testing can complete a Bio Physical Score (BPP) with a home-use ultrasound with remote clinician guidance.

What is the current status of trial NCT06442358?

This trial is currently completed. It is a NA study. The enrollment target is 25 participants. The study started on 2024-04-10. Estimated completion is 2024-12-30.

What conditions does trial NCT06442358 study?

This clinical trial studies the following conditions: Perinatal Care.

What interventions are being tested in trial NCT06442358?

The interventions under investigation include: Pulsenmore ES home ultrasound device (DEVICE).

Who is sponsoring clinical trial NCT06442358?

This trial is sponsored by PulseNmore, which has 3 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT06442358 being conducted?

This trial has 1 study location across Michigan. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

How this trial's enrollment target compares

Where NCT06442358's enrollment target sits among peer trials

25 1712th of 2000 higher than 265 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 NCT06442358, the US trial registry maintained by the National Library of Medicine. NCT06442358 (small enrollment · single site footprint · completed) retrieved and formatted by PlainTrial, see methodology.