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Collaboration Live

Philips logo

Philips

Status

Completed

Conditions

Pregnancy Related

Treatments

Device: Non-diagnostic software solution

Study type

Interventional

Funder types

Industry

Identifiers

NCT04243369
US-GIS-10649

Details and patient eligibility

About

Collaboration Live is a prospective, single-arm clinical study of subjects who provide written consent. Subjects are scanned using a Philips EPIQ 5 or EPIQ 7 Ultrasound System equipped with Collaboration Live software. The study investigator will evaluate performance of the Collaboration Live tool with regard to performance of conferencing, sharing and control capabilities. Adverse events will be reported and the study investigator will assess potential relationship to the study device or study procedure. Additionally, the utility of Collaboration Live in remote consult of study patients will be evaluated. No patient follow-up beyond the initial consultation will be conducted with the Collaboration Live software solution.

Enrollment

30 patients

Sex

Female

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Subject is at least 18 years of age
  • Subject in indicated for a routine Obstetrics/Gynecology ultrasound examination at the site.
  • Subject is willing and capable of providing informed consent and participating in this study

Exclusion criteria

  • A medical condition or co-morbidity that would be unduly affected by study participation, per investigator discretion

Trial design

Primary purpose

Health Services Research

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

30 participants in 1 patient group

Experimental - Collaboration Live software
Other group
Treatment:
Device: Non-diagnostic software solution

Trial documents
2

Trial contacts and locations

3

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Data sourced from clinicaltrials.gov

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