Recruiting NCT05913609
Safety and Effectiveness of the Yaari Extractor for Management of Shoulder Dystocia
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: Yaari Extractor.
- Who it may be relevant to
- Registry conditions: Shoulder Dystocia. Basic parameters: from 18 years · Female.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- United States
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Official title
IDE Clinical Study to Evaluate the Safety and Effectiveness of the Yaari Extractor for Management of Shoulder Dystocia
Overview
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.
Interventions
- Device Yaari Extractor
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.
Primary outcome measures
- Number of successful neonate deliveries with the Yaari Extractor device [Time frame: immediately after the intervention]
- Time interval (minutes) from the diagnosis of the shoulder dystocia until the neonate's delivery [Time frame: immediately after the intervention]
- Maternal and neonatal adverse events [Time frame: through study completion, an average of 5 days]
Secondary outcome measures (1)
- Ease of Use 5 point Likert scale User Questionnaire [Time frame: immediately after the intervention]
Eligibility criteria
Inclusion criteria
- Subject 18 years of age or older at time of consent.
- Subject planning on vaginal birth.
- Singleton pregnancy in vertex presentation.
- Full-term pregnancy having completed 37 weeks or more gestational weeks.
- Able and willing to provide written informed consent prior to enrollment.
- In the opinion of the Investigator, the subject has sufficient mental capacity to understand the informed consent form (ICF).
- Subject with fetus experiencing shoulder dystocia as defined by ACOG Practice Bulletin 178 "Shoulder dystocia is most commonly diagnosed as failure to deliver the fetal shoulder(s) with gentle downward traction on the fetal head, requiring additional maneuvers to effect delivery."
Exclusion criteria
- Patients who have undergone attempted delivery using ancillary standard of care maneuvers, to include first-line maneuvers (McRoberts ± suprapubic pressure with downward traction on the fetal head), prior to use of the Yaari Extractor. (NOTE: Hyperflexion of the hips or legs is allowed prior to and during use of the Yaari Extractor.)
- Cesarean section is planned for the patient.
- Obstetric contraindications to vaginal birth.
- Subject carrying fetus with known significant chromosomal or structural anomalies.
- Clinically estimated fetal weight ≥5kg in non-diabetic subjects.
- Clinically estimated fetal weight ≥4.5kg in subjects with diabetes.
- Subject has any general health condition or systemic disease that may represent, in the opinion of the Investigator, a potential increased risk associated with device use or pregnancy.
- Bleeding disorders, such as thrombocytopenia, von Willebrand's disease, bleeding disorder currently using anticoagulation medication, etc.
- Any maternal disease or disorder that precludes the subject from pushing effectively.
- If the maternal cervix is not fully dilated.
- If the fetal head is not completely out of the birth canal.
- In the presence of a non-reducible nuchal cord.
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: Yes
Study design
- Allocation
- Non-randomized
- Model
- Parallel assignment
- Masking
- Open label
- Primary purpose
- Treatment
Study locations
United States · 4 centers
- University of Miami - Jackson Memorial — Miami
- Rosemark WomenCare Specialist — Idaho Falls
- Unified Women's Clinical Research — Winston-Salem
- Inova Fairfax Medical Campus — Falls Church
Identifiers
NCT: NCT05913609 · CLT-005