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Russian Extreme Hypertriglyceridemia Registry

Наблюдательное Hypertriglyceridemia

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: Hypertriglyceridemia. Базовые параметры: Без ограничений · 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
Россия
Следующий шаг
Сохраните исследование, покажите его лечащему врачу и уточните актуальный статус у исследовательского центра. Расходы, документы и поездка →
Официальное название

Russian Extreme Hypertriglyceridemia Registry (REGGI)

Обзор

The REGGI registry is a prospective, multicenter observational registry in Russia designed to collect data on patients with extreme hypertriglyceridemia (triglyceride levels ≥10 mmol/L). The registry aims to describe the clinical, demographic, and molecular-genetic characteristics of patients, as well as current diagnostic approaches and treatment patterns in real-world practice. The collected data may inform future research and support improvements in patient care.

Подробное описание

Hypertriglyceridemia (HTG) is associated with an increased risk of atherosclerotic cardiovascular disease, acute pancreatitis, and all-cause mortality. The risk increases with higher triglyceride levels and is most significant in extreme HTG (triglyceride concentration ≥10 mmol/L). Epidemiological studies in the Russian Federation report a prevalence of extreme HTG of approximately 0.1-0.2% (146,000-292,000 individuals). Extreme HTG can have monogenic or polygenic (multifactorial) origins, which influences the clinical course of the disease.

Written informed consent is obtained from the patient or their legal guardian prior to inclusion.

Data sources include routine diagnostic findings and medical records. Participating sites monitor patients' clinical status as part of routine medical care. There are no interventions in this registry: medications are not changed, no invasive procedures are performed, and no study-specific interventions or procedures associated with additional risk are performed. Only clinical course, laboratory results, lipid profile, and therapeutic measures are documented, including any genetic testing if available.

Patients are followed annually or more frequently if clinically indicated. There is no minimum or maximum age for inclusion, and follow-up duration is not predefined and depends on clinical practice. Participation is voluntary, and patients may withdraw at any time without affecting their medical care. Data are pseudonymized and can be decrypted using a separately maintained key list; data can be deleted upon patient request.

Первичные конечные точки

  • Mortality (all-cause and cardiovascular) [Срок оценки: Baseline and through study completion, an average of 20 years]
Вторичные конечные точки (8)
  • Major Cardiovascular Events (MACE) [Срок оценки: Baseline and through study completion, an average of 20 years]
  • Pancreatitis Recurrences [Срок оценки: Baseline and through study completion, an average of 20 years]
  • Pancreatic Necrosis [Срок оценки: Baseline and through study completion, an average of 20 years]
  • Low-Density Lipoprotein Cholesterol (LDL-C) [Срок оценки: Baseline and through study completion, an average of 20 years]
  • Triglyceride [Срок оценки: Baseline and through study completion, an average of 20 years]
  • Total Cholesterol [Срок оценки: Baseline and through study completion, an average of 20 years]
  • High-Density Lipoprotein Cholesterol (HDL-C) [Срок оценки: Baseline and through study completion, an average of 20 years]
  • Genetic Characterization of Extreme Hypertriglyceridemia [Срок оценки: Baseline (at the time of genetic testing) and during follow-up if additional genetic data become available, through study completion (an average of 20 years).]

Критерии участия

Критерии включения

  • Patients with extreme hypertriglyceridemia (triglyceride levels ≥10 mmol/L), confirmed by at least two independent measurements.
  • Written informed consent from the patient or legal guardian.
  • No age restrictions.

Критерии исключения

  • Patients whose extreme hypertriglyceridemia is caused by alcohol abuse, uncontrolled diabetes, or other medical conditions, unless extreme hypertriglyceridemia is confirmed after controlling the underlying condition.
  • Lack of informed consent.

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

Здоровые добровольцы: Нет

Дизайн исследования

Модель наблюдения
Когортное

Центры проведения

Россия · 6 центров
  • Astrakhan State Medical University — Astrakhan
  • Chelyabinsk State Medical Academy — Chelyabinsk
  • Kaluga City Clinical Hospital No. 5 — Kaluga
  • State Medical University — Kazan'
  • National Medical Research Center of Cardiology Named after Academician E.I. Chazov — Moscow
  • Research Centre for Medical Genetics — Moscow

Идентификаторы

NCT: NCT07508930 · REGGI-HTG-2025

Первоисточники (государственные реестры)

Открыть это исследование на ClinicalTrials.gov ↗