An interventional study of Yaari Extractor in Shoulder Dystocia, sponsored by FetalEase Ltd.. Recruiting at 4 sites in United States. Open to female participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2025-11-25.
Sponsored by FetalEase Ltd. · Not applicable, Interventional, and Treatment
Prospective, multi-center, single arm with historical control, to verify the safety and effectiveness of the Yaari Extractor used by board certified or board eligible U.S. OB/GYN physicians in the management of shoulder dystocia.
This is the only study on the registry with FetalEase Ltd. as lead sponsor.
Counted across the registry records on this site, refreshed daily.
Exclusion Criteria:
Prospective experimental arm
Device: Yaari Extractor
Historical control arm - retrospective review of medical records at the same study sites
The Yaari Extractor device is a single-use prescription device for neonatal extraction in deliveries that are complicated by shoulder dystocia. The Study Device consists of two curved, rigid plastic-coated metal Arms with Handles which are used for control of the device outside the body, and an elastic Engagement Element which conforms to the maternal and neonatal anatomy, and which is used for direct contact with the entrapped neonate within the birth canal.
Number of successful neonate deliveries with the Yaari Extractor device
First Primary Effectiveness Endpoint
Time frame: immediately after the intervention
Time interval (minutes) from the diagnosis of the shoulder dystocia until the neonate's delivery
Second Primary Effectiveness Endpoint
Time frame: immediately after the intervention
Maternal and neonatal adverse events
Primary Safety Endpoint
Time frame: through study completion, an average of 5 days
Ease of Use 5 point Likert scale User Questionnaire
Secondary Effectiveness Endpoint
Time frame: immediately after the intervention
Plan to share: No
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Shoulder Dystocia