Идёт набор NCT04634916

Post-market Surveillance Study of the BD® WavelinQ™ EndoAVF System

Без фазы С лечением Kidney Disease, End-Stage End-stage Renal Disease Arteriovenous Fistula

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: EndoAVF Creation.
Кому может быть актуально: Состояния в реестре: Kidney Disease, End-Stage, End-stage Renal Disease, Arteriovenous Fistula. Базовые параметры: от 18 лет · Все.
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, Австралия
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

A Prospective, Multi-Center Clinical Study of the BD® WavelinQ™ EndoAVF System for the Creation of Arteriovenous (AV) Fistula in Patients Requiring Dialysis

Обзор

A prospective, single-arm, multi-center post-market surveillance study of the BD® WavelinQ™ EndoAVF System for the Creation of Arteriovenous (AV) Fistula in Patients Requiring Dialysis.

Вмешательства

Устройство EndoAVF Creation
Subjects will have an endoAVF created using the WavelinQ EndoAVF System

Первичные конечные точки

Functional Cannulation Success [Срок оценки: 6-months post index procedure]
Primary Patency [Срок оценки: 6-months post index procedure]
Device- and procedure-related serious adverse events (SAE) [Срок оценки: 30-days post index procedure]

Вторичные конечные точки (12)

Physiological Maturation [Срок оценки: 2-weeks, 6-weeks, 6-months, and 24-months post index procedure]
Functional Maturation [Срок оценки: 6-weeks, 3-, 6-, 12-, 18-, and 24-months post index procedure]
Procedure Success [Срок оценки: Index procedure]
Cannulation Success [Срок оценки: 6-weeks, 3-, 6-, 12-, 18-, and 24-months post index procedure]
Primary Patency [Срок оценки: 6-weeks, 3-, 12-, 18-, and 24-months post index procedure]
Assisted Primary Patency [Срок оценки: 6-weeks, 3-, 6-, 12-, 18-, and 24-months post index procedure]
Secondary Patency [Срок оценки: 6-weeks, 3-, 6-, 12-, 18-, and 24-months post index procedure]
Functional Patency [Срок оценки: through 24-months]
Functional Cannulation Success [Срок оценки: 3-, 12-, 18-, and 24-months post index procedure]
CVC Exposure/Use [Срок оценки: 6-weeks, 3-, 6-, 12-, 18-, and 24-months post index procedure]
Procedural Adjunctive Procedures [Срок оценки: Index Procedure]
Post Procedural Secondary Procedures [Срок оценки: 2-weeks, 6-weeks, 3-, 6-, 12-, 18-, and 24-months post index procedure]

Критерии участия

Критерии включения

Subject must be either male or non-pregnant female ≥ 18 years of age with an expected lifespan sufficient to allow for completion of all study procedures.
Subject must voluntarily sign and date the Informed Consent Form (ICF) prior to collection of study data or performance of study procedures.
Subject must be willing to comply with the protocol requirements, including clinical follow-up.
Subjects who have established, non-reversible kidney failure, who are currently on dialysis at screening or are in immediate need (within 6 months of endoAVF creation) of dialysis.
Target treatment vein diameter(s) for endoAVF creation ≥ 2.0 mm as measured via Duplex Ultrasound (DUS) or Venography.
Target treatment artery diameter ≥ 2.0 mm as measured via Duplex Ultrasound (DUS) or Arteriogram.
Subject has adequate collateral circulation to the hand, in the opinion of the Investigator.
At least one superficial outflow vein diameter ≥ 2.5 mm and in communication with the target creation site via a proximal forearm perforating vein.

Критерии исключения

The subject is in a hypercoagulable state.
The subject has known bleeding diathesis.
The subject has insufficient cardiac output to support a native fistula in the opinion of the Investigator.
Known history of active intravenous drug abuse.
"Planned" major surgical procedure within 6 months following index procedure or major surgery within 30 days prior to index procedure.
The subject has a known allergy or hypersensitivity to contrast media which cannot be adequately pre-medicated.
The subject has known adverse effects to sedation and/or anesthesia which cannot be adequately pre-medicated.
Evidence of active infection on the day of the index procedure (temperature of ≥ 38.0° Celsius and/ or WBC of ≥ 12,000 cells/ μL, if collected).
The subject has another medical condition, which, in the opinion of the Investigator, may cause him/her to be non-compliant with the protocol, confound the data interpretation, or is associated with a life expectancy insufficient to allow for the completion of study procedures and follow-up.
The subject is currently participating in an investigational drug or another device study that has not completed the study treatment or that clinically interferes with the study endpoints. Note: Studies requiring extended follow-up visits for products that were investigational, but have since become commercially available, are not considered investigational studies.
The subject has central venous stenosis or central vein narrowing > 50% based on imaging on the same side as the planned endoAVF creation.
Absence of a proximal forearm perforating vein feeding the target cannulation vein(s) from the target creation site via Duplex Ultrasound (DUS) or Venography.
Occlusion or stenosis > 50% of target cannulation vein(s) such as cephalic, median cubital, basilic, etc. assessed via Duplex Ultrasound (DUS) or Venography.
Significantly compromised venous or arterial flow in the treatment arm as determined by Investigator and Duplex Ultrasound (DUS) or Venography.
Presence of significant calcification at the target endoAVF location that could potentially impact the effectiveness of endoAVF creation as determined by the Investigator.

Критерии приведены из реестра в оригинале (на английском). Окончательную оценку соответствия проводит исследовательский центр.

Здоровые добровольцы: Нет