AUD Biomarkers Study (Proteomic and Genomic Analysis of Biospecimens)
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: Observational Study Only. NO Intervention..
- Кому может быть актуально
- Состояния в реестре: Oncology, Hematologic Malignancy, Gastro-Intestinal Disorder, Autoimmune Diseases. 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
- США
- Следующий шаг
- Сохраните исследование, покажите его лечащему врачу и уточните актуальный статус у исследовательского центра. Расходы, документы и поездка →
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Официальное название
AUD Biomarkers Study (Proteomic and Genomic Analysis of Biospecimens Involved in Diseases and Healthy Populations)
Обзор
Study purpose: to explore the entire spectrum of proteomic and genomic changes (amongst others) involved in diseases and in healthy/control populations. The Study is designed to discover biomarkers, develop and validate diagnostic assays, instruments and therapeutics as well as other medical research. Specifically, researchers may analyze proteins, RNA, DNA copy number changes, including large and small (1,000-100,000 kb) scale rearrangements, transcription profiles, epigenetic modifications, sequence variation, and sequence in both diseased tissue and case-matched germline DNA from Subjects.
Подробное описание
The primary objective of this Study is to collect high-quality tissue, whole teeth, and biofluid Specimens, and associated Clinical Data from consented Subjects.
The secondary objective of this Study is to test Specimens and associated Clinical Data to confirm pathology diagnosis and correlation of microscopic evaluation with the provided information, to assess RNA and DNA integrity or degradation, and provide overall quality control evaluations.
Вмешательства
- Другое Observational Study Only. NO Intervention.
Observational Study Only. NO Intervention.
Первичные конечные точки
- Enrollment and collection totals for a diverse population of subjects/conditions involved in diseases and in healthy/control populations. [Срок оценки: Through study completion, an average of once per year]
Критерии участия
Критерии включения
- Subject shall be at least 18 years of age, or higher if required by Applicable Law.
- Subject's Clinical Data shall be relevant to the Study in which he/she is participating.
- Subject shall understand and voluntarily sign the ICF prior to the Study participation. If the Subject is illiterate, the witness must sign the ICF (see 5.6. for details). If the Subject is incapable of consenting himself/herself, the legally authorized representative must sign the ICF (see 5.6. for details).
- Subject shall meet any other additional inclusion criteria specified in Appendices to this Protocol, or in additional written instructions of the Sponsor.
- Subject shall be able to donate the requested Specimen(s) without compromising his/her current health status.
Критерии исключения
- Younger than 18 years of age, or higher if required by Applicable Law.
- The individual is incapable of understanding the items listed in the ICF and the consent process unless consented by the legally authorized representative.
- Prisoner
Критерии приведены из реестра в оригинале (на английском). Окончательную оценку соответствия проводит исследовательский центр.
Здоровые добровольцы: Да
Дизайн исследования
- Модель наблюдения
- Когортное
Центры проведения
США · 1 центр
- AUD — New Orleans
Идентификаторы
NCT: NCT05889806 · US005