Resource Center

This section contains international research and may reference indications not approved in all regions. Please consult local approved indications before use.

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The study discussed the use of tele-ultrasound for fetal assessment in regions affected by crisis and conflict. It highlighted how remote ultrasound technology could provide crucial prenatal care in resource-limited
In this pilot study, patient-operated remote ultrasonography was feasible for completing BPPs in high-risk pregnancies. This new technology may improve access to critical antenatal surveillance services, particularly for patients facing
Abstract Objective To evaluate the feasibility and accuracy of remote, clinician-guided biophysical profile (BPP) assessment using a handheld ultrasound device operated by lay users. Methods This prospective, non-randomized, quasi-blinded study
Our findings demonstrate that self-administered fetal tele-ultrasound is feasible and associated with high user satisfaction and usability. This study supported its potential as a complementary tool in obstetric care, highlighting
Integrating routine home-ultrasound telemedicine visits into prenatal care can significantly reduce maternal anxiety during pregnancy and contribute to greater maternal attachment in women with a history of recurrent pregnancy loss.
Home ultrasound and CTG are potentially feasible and acceptable to high-risk pregnant women. Larger studies are required to refine how best to implement such devices within clinical practice. To our
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FAQ

Frequently asked question

No, the Clinician-Dashboard interface is an online web application that utilizes an active directory access technology (permission management tool).

Data is available for review for 30 days. During this time, the HCP can download and save the scans onto the patient file. More information is available in our Terms of Use.

Pulsenmore utilizes service logs and technical information to improve services and enhance user experience. De-identified data is used for clinical education, training, research and development purposes only.

The device is designed for a single patient use, to prevent cross contamination.

The health care provider determines the maximum amount of scans that can be performed by the user. The device is limited to up to 50 scans per pregnancy.

Pulsenmore collects four types of data:

• Service logs: Application usage logs, such as performance logs and errors.

• Technical information about the smartphone: Smartphone capabilities, application version, language, etc.

• Interpreter Data: The identifiers of the clinicians that interpret the scans.me, scan measurements and last menstrual period (LMP).

You can view the scan in real-time while following the scanning instructions in the app. After the scan, the images are sent to the doctor and cannot be reviewed again.

Every scan requires medical interpretation, and its important to wait until the files are fully uploaded. You are not expected to understand or interpret the ultrasound scans; follow the app’s instructions to scan, and receive a response from skilled ultrasound professionals .

Yes, the device is reliable and was tested, validated and approved for use in the US, Europe, Australia, Brazil, Switzerland, the UK, Colombia and Israel. Over 200,000 successful scans have been performed since the launch of the technology. These numbers demonstrate that women can confidently scan themselves, as the diagnoisis it self is being done by a trained clinical team. The remote clinical team can accurately identify parameters related to fetal vitality, such as fetal heartbeat based on these scans.

Yes. Pulsenmore is based on the same ultrasound technology used routinely in clinics. Scans are performed within established safety guidelines and reviewed by a medical professional, so you receive reliable clinical insight while maintaining the safety of both you and your baby.