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NCT05329077 · ClinicalTrials.gov registry record · NA
Pulsenmore ES Device, Efficacy and Safety Assessment
A NA study, sponsored by PulseNmore.
- Completed
- Registry status
- NA
- Development phase
- 188
- Enrollment target
NCT05329077: Completed NA study, sponsored by PulseNmore.
NCT05329077 is a NA study that has completed, run by PulseNmore. The registered enrollment target is 188 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (87% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT05329077, a NA study, has completed, sponsored by PulseNmore.
- COMPLETED
- Registry status
- NA
- Development phase
- 188 participants
- Enrollment target
Study Summary
This is a multicenter, prospective, investigational device study designed to evaluate: The safety, feasibility, and accuracy of the device, when used by pregnant individuals
Primary Outcome
The presence or absence of device derived fetal cardiac activity would be matched with the presence or absence of fetal cardiac activity derived by the ground truth (in-clinic ultrasound scan)
Interventions
- DEVICE Pulsenmore ES home ultrasound device
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 188 participants |
| Start Date | 2022-04-14 |
| Est. Completion | 2023-11-11 |
| Phase | NA |
What the finished NCT05329077 record still lists
NCT05329077 is an interventional study that assigns participants to a tested intervention. The registered 188 participants enrollment target is mid-sized for trials with a published cap, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (87% lower).
The record links to 0 conditions, and to 1 intervention - of which Pulsenmore ES home ultrasound device is the first listed.
NCT05329077 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT05329077 about?
NCT05329077 is a clinical study titled "Pulsenmore ES Device, Efficacy and Safety Assessment". This is a multicenter, prospective, investigational device study designed to evaluate: The safety, feasibility, and accuracy of the device, when used by pregnant individuals
What is the current status of trial NCT05329077?
This trial is currently completed. It is a NA study. The enrollment target is 188 participants. The study started on 2022-04-14. Estimated completion is 2023-11-11.
What interventions are being tested in trial NCT05329077?
The interventions under investigation include: Pulsenmore ES home ultrasound device (DEVICE).
Who is sponsoring clinical trial NCT05329077?
This trial is sponsored by PulseNmore, which has 3 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT05329077's enrollment target sits among peer trials
188 576th of 2000 higher than 1,422 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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