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Идёт набор NCT07430293

Hybrid Closed-Loop Insulin Delivery After Pancreatectomy

Без фазы С лечением Pancreatectomy Total Pancreatectomy Partial Pancreatectomy

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: MiniMed 780 associated with Simplera.
Кому может быть актуально
Состояния в реестре: Pancreatectomy, Total Pancreatectomy, Partial Pancreatectomy. 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
Франция
Следующий шаг
Сохраните исследование, покажите его лечащему врачу и уточните актуальный статус у исследовательского центра. Расходы, документы и поездка →
Официальное название

Metabolic Effects of Hybrid Closed-loop Insulin Delivery in People With Diabetes After Pancreatectomy: a Randomized Cross-over Controlled Trial

Обзор

Individuals with diabetes secondary to pancreatectomy experience impaired quality of life, partly due to the challenges of managing highly variable blood glucose levels. Hybrid closed-loop (HCL) automated insulin delivery (AID) systems, widely evaluated in type 1 diabetes, may improve both metabolic outcomes and quality of life in this population. A review of the literature identified a few observational studies reporting promising results with HCL systems in the context of post-pancreatectomy diabetes. Only one randomized trial has evaluated AID in this population, showing excellent outcomes, but using a complex bihormonal system that is not yet commercially available worldwide. Consequently, there remains a lack of confirmatory evidence regarding the efficacy of commercially available monohormonal HCL systems in individuals with diabetes secondary to pancreatectomy, evidence that is crucial to support broader access to this technology. The intervention will consist in a 3-month AID treatment combining MiniMed 780 and Simplera. The control period will consist in 3 months using the Simplera for continuous glucose monitoring, alongside participant usual diabetes treatment. The primary outcome is the percentage of time that interstitial glucose levels remain within the target range (70-180 mg/dL), as measured by continuous glucose monitoring (CGM, Simplera), over a 3-month period using the MiniMed 780 hybrid closed-loop system, compared to a 3-month period under the participant's usual diabetes treatment.

Подробное описание

The MiniMed 780G system comprises an external insulin pump with a subcutaneous infusion catheter inserted by the participant using a dedicated insertion kit. The infusion set is placed in the abdomen, buttocks, thighs, or upper arms, following standard hygiene procedures.

The Simplera system consists of an all-in-one external continuous glucose sensor inserted subcutaneously in the back of the upper arm via a dedicated insertion device.

Вмешательства

  • Устройство MiniMed 780 associated with Simplera
    MiniMed 780 associated with Simplera

Первичные конечные точки

  • Percentage of time in range [Срок оценки: At 3 months]
Вторичные конечные точки (4)
  • HbA1c [Срок оценки: At 3 months]
  • Percentage of time below range [Срок оценки: At 3 months]
  • Glucose coefficient of variation [Срок оценки: At 3 months]
  • Frequency of acute metabolic events [Срок оценки: At 3 months]

Критерии участия

Критерии включения

  • Age from 18 years
  • History of total or partial pancreatectomy with random C-peptide < 0.3 ng/mL and concomitant blood glucose between 120 and 225 mg/dL (no minimum delay required since surgery)
  • Total daily insulin dose between 6 units and 250 units
  • Be affiliated to a French social security scheme
  • Individual able and willing to provide written informed consent

Критерии исключения

  • Presence of diabetic retinopathy at or beyond severe non-proliferative diabetic retinopathy, not stabilized by ophthalmologic treatment
  • Usual diabetes treatment with an insulin pump coupled with continuous glucose monitoring with a "suspend before hypoglycemia" system
  • Pregnant woman or planned pregnancy within the next 6 months
  • Ongoing or planned chemotherapy that interferes or is expected to interfere with glycemic control or nutritional intake, particularly in cases of clinically significant gastrointestinal toxicity and/or associated systemic corticosteroid therapy, after consultation with the treating oncologist.
  • Enteral or parenteral nutrition
  • Estimated life expectancy less than 12 months
  • Cognitive or psychiatric disorders compromising the individual's autonomy to manage automated insulin delivery
  • Person taking part in another research study or with an exclusion period still in progress
  • Individual under legal guardianship or curatorship
  • Any contraindication mentioned in the instructions for use of the MiniMed 780 - Simplera
  • Imprisoned or otherwise deprived of liberty

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

Здоровые добровольцы: Нет

Дизайн исследования

Распределение
Рандомизированное
Модель
Перекрёстный дизайн
Маскирование
Открытое
Основная цель
Лечение

Центры проведения

Франция · 2 центра
  • Centre Hospitalier Sud Francilien — Corbeil-Essonnes
  • Hôpital Bichat (APHP) — Paris

Идентификаторы

NCT: NCT07430293 · 2025-A02384-45

Первоисточники (государственные реестры)

Открыть это исследование на ClinicalTrials.gov ↗