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Набор скоро начнётся NCT07684690

AI-Assisted Antidiabetic Drug Consultation System for Glycemic Control in Type 2 Diabetes Patients Managed by Non-Specialist Physicians

Без фазы С лечением Type 2 Diabetes Mellitus (T2DM)

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: AI-assisted antidiabetic drug consultation system, Manual antidiabetic prescribing (without AI).
Кому может быть актуально
Состояния в реестре: Type 2 Diabetes Mellitus (T2DM). Базовые параметры: 19 лет — 80 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
Тайвань
Следующий шаг
Сохраните исследование, покажите его лечащему врачу и уточните актуальный статус у исследовательского центра. Расходы, документы и поездка →
Официальное название

Clinical Validation of AI-assisted Antidiabetic Drug Consultation System-1

Обзор

This study tests whether an artificial intelligence (AI) tool can help doctors choose better diabetes medicines for their patients. Type 2 diabetes is very common, but there are far more patients than diabetes specialists, so many patients are treated by doctors who are not diabetes specialists. The researchers built an AI consultation system that gives doctors real-time suggestions and predictions about diabetes medicines while they are prescribing. The doctor always makes the final decision. In this trial, patients with type 2 diabetes whose blood sugar is not well controlled will be placed by chance (randomly) into one of two groups. In one group, the doctor uses the AI system when deciding on diabetes medicines. In the other group, the doctor prescribes as usual, without the AI system. All medicines used are already approved in Taiwan and given at approved doses. The study follows each patient for 12 months, with check-ups at the start and at 3, 6, 9, and 12 months. The main goal is to compare how much the patients' long-term blood sugar level (HbA1c) improves between the two groups after one year. The researchers also look at how many patients reach their blood sugar target, how often low blood sugar happens, and whether any side effects occur. The aim is to find out whether using the AI tool leads to better blood sugar control.

Вмешательства

  • Устройство AI-assisted antidiabetic drug consultation system
    A machine-learning based clinical decision support software that provides non-specialist physicians with real-time, interactive antidiabetic prescribing recommendations, a drug-prioritization order, and outcome predictions (e.g., the predicted likelihood of reaching glycemic targets and responder/non-responder status for individual drugs). The system was developed and validated using the NTUH integrated medical database platform. It provides advisory recommendations only; the treating physician
  • Другое Manual antidiabetic prescribing (without AI)
    Antidiabetic medications prescribed manually by non-specialist physicians according to usual clinical practice, without using the AI consultation system. All medications are approved in Taiwan and prescribed within approved dose ranges.

Первичные конечные точки

  • Change in HbA1c from baseline to 12 months [Срок оценки: Baseline and 12 months]
Вторичные конечные точки (4)
  • Proportion of participants achieving HbA1c < 7.0% at 12 months [Срок оценки: 12 months]
  • Incidence of hypoglycemia over 12 months [Срок оценки: Up to 12 months]
  • Incidence of prespecified adverse events over 12 months [Срок оценки: Up to 12 months]
  • Change in HbA1c from baseline at 3, 6, 9, and 12 months [Срок оценки: Baseline, 3, 6, 9, and 12 months]

Критерии участия

Критерии включения

  • Adults aged 18 to 80 years
  • Diagnosis of type 2 diabetes for at least 6 months
  • HbA1c above 8% within the past 3 months
  • Currently using one or more oral antidiabetic drugs
  • Able to understand and provide written informed consent

Критерии исключения

  • Pregnancy or breastfeeding
  • Recent participation in another interventional clinical trial
  • Cognitive impairment precluding understanding of the study
  • Active cancer treatment within the past 6 years
  • Use of systemic steroids

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
Простое слепое
Основная цель
Лечение

Центры проведения

Тайвань · 1 центр
  • National Taiwan University Hospital — Taipei

Идентификаторы

NCT: NCT07684690 · 202507154RINA · 115-X007

Первоисточники (государственные реестры)

Открыть это исследование на ClinicalTrials.gov ↗