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Набор по приглашению NCT04966858

Individualized Study of Refeeding to Optimize iNpatient Gains

Без фазы С лечением Atypical Anorexia Nervosa

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: Individualized Caloric Refeeding (ICR), Higher Calorie Refeeding (HCR).
Кому может быть актуально
Состояния в реестре: Atypical Anorexia Nervosa. Базовые параметры: 12 лет — 24 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
США
Следующий шаг
Сохраните исследование, покажите его лечащему врачу и уточните актуальный статус у исследовательского центра. Расходы, документы и поездка →
Официальное название

Renewal of the Multi-center Randomized Controlled Trial of Refeeding in Anorexia Nervosa

Обзор

The primary purpose of the trial is to compare the efficacy and safety of Individualized Caloric Refeeding (ICR) to the new standard of care, Higher Calorie Refeeding (HCR), in hospitalized patients with atypical anorexia nervosa (AAN), and clinical remission over one year of follow-up.

Подробное описание

Atypical Anorexia Nervosa (AAN) is a new diagnosis describing patients with malnutrition and significant weight loss yet "normal" weight. These patients responded poorly to HCR, the superior refeeding treatment in the parent trial, which was designed for low-weight patients with typical AN. The proposed trial will examine the safety and efficacy of a new treatment for AAN with the potential to improve treatment outcomes for this diverse and growing patient population. The major finding motivating the proposed trial is that participants with AAN gained weight 40 percent slower and required 3.0 additional days in hospital to restore medical stability on HCR, as compared to AN. The research team has developed Individualized Caloric Refeeding (ICR), which doses calories to weight consistent with other pediatric treatments (e.g. medication).

The primary purpose of the proposed trial is to compare the efficacy and safety of ICR to the new standard of care (HCR) in hospitalized patients with AAN. The investigators hypothesize that ICR will restore medical stability faster than HCR with no increase in electrolyte abnormalities. After hospitalization, the major barrier to care in AAN is lack of consensus on clinical remission and whether these formerly overweight patients should gain weight to recover. The research team will examine metabolic, hormonal and psychological markers during long-term follow-up, toward the goal of developing a definition of clinical remission in AAN.

Design Summary: Randomized controlled trial in N=74 participants age 12-24 with AAN, consented upon hospital admission, randomly assigned to ICR or HCR, followed daily in hospital and at 3, 6, 9 and 12 mo.

Вмешательства

  • Другое Individualized Caloric Refeeding (ICR)
    Meal-based refeeding in hospital, starting at 50 calories per kilogram of body weight, and increasing by 200 calories per day until caloric goal achieved
  • Другое Higher Calorie Refeeding (HCR)
    Meal-based refeeding in hospital, starting at 2000 calories per day, and increasing by 200 calories per day until caloric goal achieved

Первичные конечные точки

  • Time to Achieve Medical Stability in Hospital [Срок оценки: Inpatient hospitalization from day of admission to day of discharge, average 1-2 weeks]
Вторичные конечные точки (1)
  • Incidence of low serum electrolytes during refeeding in hospital [Срок оценки: Inpatient hospitalization from day of admission to day of discharge, average 1-2 weeks]

Критерии участия

Критерии включения

  • Age 12-24 yrs
  • Meets Diagnostic and Statistical Manual of Mental Disorders (DSM-5) criteria for AAN
  • Hospitalized with medical instability, as defined by:
  • night time heart rate (HR) <45 bpm,
  • systolic blood pressure (SBP) <90 mmHg,
  • temperature <35.6° C,
  • orthostatic Δ HR >35 bpm, or
  • orthostatic Δ SBP >20 mmHg

Критерии исключения

  • Bulimia nervosa
  • Current pregnancy
  • Chronic disease (e.g. immune, renal disease)
  • Acute/active suicidality or psychosis
  • Hospital admissions for refeeding in the prior 6 mo.

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
Открытое
Основная цель
Лечение

Центры проведения

США · 2 центра
  • Stanford University Lucille Packard Children's Hospital — Palo Alto
  • University of California, San Francisco Benioff Children's Hospital — San Francisco

Идентификаторы

NCT: NCT04966858 · 2R01HD082166-06A1 · 20-32551 · R01HD082166 · HD082166 · P0547076

Первоисточники (государственные реестры)

Открыть это исследование на ClinicalTrials.gov ↗