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Набор скоро начнётся NCT07312006

Comparison of AirSeal to DV5 Insufflation in Gastric Sleeve Procedures - The "CAT5-GS" Study

Без фазы С лечением Pain, Postoperative

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: AirSeal Insufflation system, DV5 Insufflation system.
Кому может быть актуально
Состояния в реестре: Pain, Postoperative. Базовые параметры: 22 лет — 65 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
Следующий шаг
Сохраните исследование, покажите его лечащему врачу и уточните актуальный статус у исследовательского центра. Расходы, документы и поездка →

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Обзор

A study to compare two different insufflation devices during robotic laparoscopic sleeve gastrectomy surgery, AirSeal to DV5 insufflation, in Gastric Sleeve Procedures. Shoulder, neck and chest pain will be assessed.

Подробное описание

A Single-Center, Prospective, Randomized, Controlled Study Comparing Intraoperative and Perioperative Outcomes using the CONMED AirSeal® and DV5 Insufflators during Robotic Laparoscopic Sleeve Gastrectomy.

Вмешательства

  • Устройство AirSeal Insufflation system
    AirSeal Insufflation system used during robotic sleeve gastrectomy
  • Устройство DV5 Insufflation system
    DV5 Insufflation system used during robotic laparoscopic sleeve gastrectomy.

Первичные конечные точки

  • Pain Assessment on a 0 - 10 numerical rating scale (NRS) [Срок оценки: 48 hours after surgery]
Вторичные конечные точки (1)
  • Time [Срок оценки: 1) Evening Surgery Day- (at 8 PM) 2) Morning- (Day 1 at 8:00 AM) 3) Evening- (Day 1 at 8 PM) 4) Morning -(Day 2 at 8 AM.) 5) Evening- (Day 2 at 8 PM)]

Критерии участия

Критерии включения

\- • Subject indicated for non-emergent sleeve gastrectomy surgery

  • Subjects (or appropriate legal representatives) able to provide written informed consent to participate in the study
  • Male or Female aged 22 years to 65 years
  • Have no significant psychopathology that could limit the subject's ability to understand the procedure, comply with medical, surgical, and/or behavioral recommendations and office visits
  • Agree to refrain from any type of elective procedures that would affect body weight such as abdominal lipoplasty or liposuction, mammoplasty, or removal of excess skin for the duration of the trial.
  • Are American Society of Anesthesiologists (ASA) Class I, II, or III);

Критерии исключения

  • Subject participation in a different investigational clinical study within 90 days before screening and for the duration of this trial (unless previously approved by the investigator and Sponsor)
  • Subject requiring any surgical procedure in addition to Sleeve Gastrectomy
  • Previous malabsorptive or restrictive procedures performed for the treatment of obesity
  • Inability to provide informed consent
  • Unable or unwilling to attend follow-up visits and examinations
  • Uncontrolled hypertension (Systolic: ≥180 mmHg or Diastolic: ≥120 mmHg) and/or diabetes mellitus (Fasting blood sugar level: >200 mg/dL)
  • Subject who falls into American Society of Anesthesiologists (ASA) Class ≥ IV
  • History of chronic alcohol or drug abuse within 2 years of the screening visit
  • Chronic renal failure or on dialysis
  • Significant complicating medical history or immunocompromised
  • Subject is undergoing surgery for malignant disease
  • History or presence of pre-existing autoimmune connective tissue disease, e.g., systemic lupus erythematosus or scleroderma
  • Immunocompromised such as that resulting from chronic oral steroid use, chemotherapeutic agents, or immune deficiency disorders
  • Any medical condition which precludes compliance with the study
  • Subject with any other clinically significant unstable medical disorder, life threatening disease, or conditions that, in the opinion of the investigator, may jeopardize the subject's well-being and/or the soundness of this clinical study or which would contra-indicate a surgical procedure
  • Previous or current history of being on regular analgesia / pain killers
  • Advanced refusal of blood transfusion, (if necessary)
  • If female subject pregnant, planning to become pregnant within 3 months (up to 92 days of procedure), or lactating

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

Здоровые добровольцы: Нет

Дизайн исследования

Распределение
Рандомизированное
Модель
Параллельные группы
Маскирование
Открытое
Основная цель
Лечение

Центры проведения

США · 1 центр
  • Baptist Health South Miami Hospital — Miami

Идентификаторы

NCT: NCT07312006 · DD 02250910

Первоисточники (государственные реестры)

Открыть это исследование на ClinicalTrials.gov ↗