Меню
Набор скоро начнётся NCT07501780

Real-world Evaluation of the Implementation of LC-OCT in Daily Clinical Practice

Наблюдательное Basal Cell Carcinoma of Skin Optical Coherence Tomography (OCT) Neoplasms Neoplasms, Basal Cell

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
Это наблюдательное исследование: исследуемое лечение участникам по протоколу не назначают.
Кому может быть актуально
Состояния в реестре: Basal Cell Carcinoma of Skin, Optical Coherence Tomography (OCT), Neoplasms, Neoplasms, Basal Cell. 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
Нидерланды
Следующий шаг
Сохраните исследование, покажите его лечащему врачу и уточните актуальный статус у исследовательского центра. Расходы, документы и поездка →
Официальное название

Real-world Evaluation of the Implementation of LC-OCT in Daily Clinical Practice: a Retrospective Observational Study

Обзор

Basal cell carcinoma (BCC) is the most common skin cancer in the Netherlands, with incidence rates continuing to rise. The current diagnostic standard combines clinical evaluation and dermoscopy, while biopsy followed by histopathological examination remains the gold standard when uncertainty about the diagnosis persists. However, biopsy is invasive, time-consuming, and costly. Line-field confocal optical coherence tomography (LC-OCT) is a non-invasive imaging technique that has emerged as a promising alternative to biopsy for BCC suspected lesions. This retrospective study aims to evaluate the real-world clinical performance of LC-OCT in routine dermatological practice, where it has been integrated into the diagnostic work-up for BCC-suspect lesions.

Подробное описание

Basal cell carcinoma (BCC) is the most common type of skin cancer in the Netherlands, with its incidence having increased substantially in recent years. ). Over the past decades, non-invasive imaging techniques such as line-field confocal optical coherence tomography (LC-OCT) have emerged as promising alternatives to biopsy for the diagnosis of BCC. When BCC can be diagnosed with high confidence using (LC-)OCT, this may reduce the need for biopsies, accelerate treatment initiation, and improve healthcare efficiency. LC-OCT combines the principles of conventional optical coherence tomography (OCT) and reflectance confocal microscopy (RCM), enabling three-dimensional visualization of the skin at a cellular resolution.

Several studies have reported a high specificity of LC-OCT for identifying non-BCC lesions, ranging from 97-99%. In cases where BCC can be diagnosed with high confidence, biopsy may theoretically be omitted, meaning that treatment could be initiated promptly. Reported sensitivities for such "high-confidence" BCC diagnoses range from 95-100%.

Although the diagnostic accuracy of LC-OCT has been investigated extensively in research settings, evidence on its real-world clinical performance remains limited. This retrospective study aims to evaluate the clinical utility of LC-OCT in routine dermatological practice.

Первичные конечные точки

  • Tumor free survival [Срок оценки: From enrollment to end of treatment at 6-12 months.]
Вторичные конечные точки (5)
  • Diagnostic accuracy for BCC detection [Срок оценки: From enrollment to end of treatment at 6-12 months.]
  • Treatment strategies [Срок оценки: From enrollment to end of treatment at 6-12 months.]
  • Number of performed LC-OCT scans [Срок оценки: From enrollment to 6-12 months]
  • Lesion characteristics [Срок оценки: At baseline]
  • Proportion of biopsies omitted [Срок оценки: From enrollment to end of treatment at 6-12 months.]

Критерии участия

Критерии включения

  • Patients aged ≥18 years
  • LC-OCT performed as part of diagnostic evaluation between January 2025 and June 2025 at Mohs clinics in the Netherlands
  • Histopathological results (biopsy or excision) and/or 6-12 month clinical follow-up data available

Критерии исключения

  • Patients <18 years of age
  • Cases without histopathological confirmation or available follow-up data

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

Здоровые добровольцы: Нет

Дизайн исследования

Модель наблюдения
Когортное

Центры проведения

Нидерланды · 1 центр
  • Maastricht University Medical Center + — Maastricht

Идентификаторы

NCT: NCT07501780 · METC2025-0250

Первоисточники (государственные реестры)

Открыть это исследование на ClinicalTrials.gov ↗