Safety and Effectiveness of the Yaari Extractor for Management of Shoulder Dystocia
Ориентир для пациента и семьи
Простыми словами
Автоматическая сводка по структурированным данным реестра. Она помогает сориентироваться, но не заменяет официальный протокол или оценку врача.
- Что изучают
- В протоколе указаны: Yaari Extractor.
- Кому может быть актуально
- Состояния в реестре: Shoulder Dystocia. Базовые параметры: от 18 лет · Женщины.
- Что важно проверить
- Возраст, диагноз и пол — только базовые ориентиры. Предыдущее лечение, анализы и другие обязательные условия указаны ниже в критериях участия.
- Где проводится
- США
- Следующий шаг
- Сохраните исследование, покажите его лечащему врачу и уточните актуальный статус у исследовательского центра. Расходы, документы и поездка →
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Официальное название
IDE Clinical Study to Evaluate the Safety and Effectiveness of the Yaari Extractor for Management of Shoulder Dystocia
Обзор
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.
Вмешательства
- Устройство 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.
Первичные конечные точки
- Number of successful neonate deliveries with the Yaari Extractor device [Срок оценки: immediately after the intervention]
- Time interval (minutes) from the diagnosis of the shoulder dystocia until the neonate's delivery [Срок оценки: immediately after the intervention]
- Maternal and neonatal adverse events [Срок оценки: through study completion, an average of 5 days]
Вторичные конечные точки (1)
- Ease of Use 5 point Likert scale User Questionnaire [Срок оценки: immediately after the intervention]
Критерии участия
Критерии включения
- 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."
Критерии исключения
- 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.
Критерии приведены из реестра в оригинале (на английском). Окончательную оценку соответствия проводит исследовательский центр.
Здоровые добровольцы: Да
Дизайн исследования
- Распределение
- Нерандомизированное
- Модель
- Параллельные группы
- Маскирование
- Открытое
- Основная цель
- Лечение
Центры проведения
США · 4 центра
- University of Miami - Jackson Memorial — Miami
- Rosemark WomenCare Specialist — Idaho Falls
- Unified Women's Clinical Research — Winston-Salem
- Inova Fairfax Medical Campus — Falls Church
Идентификаторы
NCT: NCT05913609 · CLT-005