Pocket-Sized ultrasound could transform pregnancy care in remote areas
NCT ID NCT05765539
First seen Jun 26, 2026 · Last updated Jun 26, 2026
Summary
This study tested a small, portable ultrasound device (echOpen O1) for pregnancy follow-ups in Senegal, where access to standard machines is limited. 224 pregnant women were scanned with both the portable device and a regular ultrasound machine to see if the portable one could reliably check fetal position, number, heartbeat, and placental location. The goal is to help midwives in low-resource areas detect complications early and improve care.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- echOpen O1 Handheld Ultrasound device
- What this could lead to
- If successful, this portable ultrasound could help midwives in remote areas detect pregnancy complications early, improving mother and baby health.
- What could go wrong
- This is a small, completed study in one country. The device may not be as accurate as standard machines, and results may not apply to other settings.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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224 people
The number who actually took part.
- Started
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Nov 2023
- Finished
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Jun 2025
- Lead sponsor
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A company
The lead sponsor is a pharmaceutical, biotech, or medical-device company.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Female participants only
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Pregnancy ≥ 37 weeks of amenorrhea * Women aged ≥ 18 years old * Delivery scheduled to take place in the recruitment center * Have given her written informed consent to participate Exclusion Criteria: * Known fetal morphological abnormality * Emergency context during the participant's management * Obstetrical work in progress * Women anticipating displacement or no delivery at the clinical site
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Centre de Santé de Sokone
Sokone, Fatick, Senegal
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Poste de Santé de Karang
Karang Poste, Fatick, Senegal
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