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Набор скоро начнётся NCT07308743

Impact of Computer-aided Detection System on the Proximal Adenoma Miss Rate

Без фазы С лечением Colon Adenomas Colon Polyps Sessile Serrated Lesion

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: Computer-aided detection-assisted colonoscopy, Conventional white-light colonoscopy.
Кому может быть актуально
Состояния в реестре: Colon Adenomas, Colon Polyps, Sessile Serrated Lesion. Базовые параметры: 40 лет — 75 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
Китай
Следующий шаг
Сохраните исследование, покажите его лечащему врачу и уточните актуальный статус у исследовательского центра. Расходы, документы и поездка →
Официальное название

Impact of Computer-aided Detection System on the Proximal Adenoma Miss Rate: a Multicenter Tandem Rondomized Controlled Trial

Обзор

This is a prospective, multicenter randomized controlled trial designed to determine whether the use of computer-aided detection system could reduce the miss rates of adenomas, SSLs, and polyps in the proximal colon during tandem colonoscopy.

Подробное описание

1. Study Centers 1) Nanfang Hospital, Southern Medical Univerisity, Guangzhou, China 2) The Fifth Affiliated Hospital of Zunyi Medical University, Zhuhai, China 3) Longgang District People's Hospital of Shenzhen, Shenzhen, China 4) Yangjiang People's Hospital, Yangjiang, China 5) Jiangmen Central Hospital, Jiangmen, China 6) Huizhou Third People's Hospital, Huizhou, China 7) Dongguan Shuixiang Central Hospital, Dongguang, China 8) Pingshan District People's Hospital of Shenzhen, Shenzhen, China 2. Study population 1) Inclusion criteria:

1. Patients age 40-75 years old, regardless of gender 2. Patients presenting for physical examination, colorectal cancer screening or diagnosis 3. Patients voluntarily signs an informed consent form 2) Exclusion criteria:

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1. Unable to cooperate ot tolerate colonoscopy 2. History of inflammatory bowel disease 3. History of colorectal cancer 4. Previous colorectal surgery 5. History of recurrent constipation 6. Taking anticoagulant and antiplatelet drugs berfore procedure 7. High risk conditions such as severe cardiovascular and cerebrovascular diseases, severe anemia, or uncorrected infections 8. Pregnant or lactating women Researchers concluded that patient was not suitable to participate in this trial.

3\) Post-randomization exclusion criteria:

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1. Cecum could not be intubated for various reasons 2. Boston Bowel Preparation Scale (BBPS) score of the proximal colon is \<2 3. Study design This is a prospective , multicenter randomized controlled trial comparing the miss rates of proximal colonic lesions (including adenomas, SSLs, and polyps) by computer-aided detection-assisted colonoscopy or conventional colonoscopy. The study will be conducted in the Endoscopy Centre of the participating hospitals. 4. Randomization 1) Eligible patients at each center will be randomized (1:1) to computer-aided detection-assisted colonoscopy first or conventional white light colonoscopy first, followed immediately by the other procedure in tandem fashion by the same endoscopist. The proximal colon is defined as the colonic segment proximal to the hepatic flexure.

2\) Randomization will be performed using computer-generated random sequences in blocks of 6, with stratification by academic level of participation center, experience of endoscopists, and indications of colonoscopy. Patients will be blinded to their group assignment.

Вмешательства

  • Устройство Computer-aided detection-assisted colonoscopy
    Computer-aided detection-assisted colonoscopy for detection of colonic polyp
  • Процедура Conventional white-light colonoscopy
    Conventional white-light colonoscopy

Первичные конечные точки

  • Proximal adenoma missed rate [Срок оценки: One day]
Вторичные конечные точки (3)
  • Proximal polyp missed rate [Срок оценки: One day]
  • Proximal SSLs missed rate [Срок оценки: One days]
  • Proximal advanced adenoma missed rate [Срок оценки: One day]

Критерии участия

Критерии включения

  • Patients age 40-75 years old, regardless of gender
  • Patients presenting for physical examination, colorectal cancer screening or diagnosis
  • Patients voluntarily signs an informed consent form

Критерии исключения

  • Unable to cooperate ot tolerate colonoscopy
  • History of inflammatory bowel disease
  • History of colorectal cancer
  • Previous colorectal surgery
  • History of recurrent constipation
  • Taking anticoagulant and antiplatelet drugs berfore procedure
  • High risk conditions such as severe cardiovascular and cerebrovascular diseases, severe anemia, or uncorrected infections
  • Pregnant or lactating women Researchers concluded that patient was not suitable to participate in this trial.

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

Здоровые добровольцы: Да

Дизайн исследования

Распределение
Рандомизированное
Модель
Параллельные группы
Маскирование
Простое слепое
Основная цель
Диагностика

Центры проведения

Китай · 1 центр
  • Nanfang Hospital, Southern Medical University — Гуанчжоу

Идентификаторы

NCT: NCT07308743 · NFEC-2025-679

Первоисточники (государственные реестры)

Открыть это исследование на ClinicalTrials.gov ↗