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Идёт набор NCT02485847

IRIS Registry: Intelligent Research in Sight Registry

Наблюдательное Eye Diseases

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: Ophthalmology.
Кому может быть актуально
Состояния в реестре: Eye Diseases. Базовые параметры: от 6 мес. · 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 →

Обзор

The IRIS™ Registry (Intelligent Research in Sight) is the nation's first comprehensive eye disease clinical registry. The American Academy of Ophthalmology is developing it as part of the profession's shared goal of continual improvement in the delivery of eye care.The IRIS Registry will be a centralized system for ophthalmology practices to promote practice innovations and achieve clinical excellence.

Подробное описание

The IRIS Registry is primarily a clinical self-improvement tool. It will allow ophthalmologists to compare their patient outcomes, professional performance and care processes against other ophthalmologists across the country. The IRIS Registry will be able to measure the continuum of care from initial patient contact, through intervention and follow up.

Improve Patient Care - Monitor patient interactions, track interventions, identify and address gaps in quality of care, and measure quality outcomes.

Manage Patient Populations - Proactively manage clinical conditions for entire patient populations by running reports on specific care criteria.

Benchmark Your Practice - Identify practice strengths and weaknesses using the IRIS Registry's ophthalmology-specific clinical data from other practices to compare to the performance and outcomes data of your practice.

Run quality reports on demand - Providing clinician- and practice-level results, plus national results and patient-level detail for all IRIS Registry measures.

Enhance Quality and Practice Efficiency - Use the IRIS Registry data to analyze practice processes and procedures and as a source for fact-based decision-making. Because the IRIS Registry will capture data over time at the individual and practice level, it will help practices efficiently manage patient care and optimize practice resources.

Join a Community of Quality - Become a member of a like-minded community of quality-driven professionals striving to continuously improve patient care. Interact with your peers to create opportunities for sharing quality improvement strategies and broaden your professional network.

Вмешательства

  • Процедура Ophthalmology
    A registry of ophthalmic ambulatory encounters which captures essential data elements for continuous quality improvement efforts, enhanced patient care outcomes, and pay for performance programs.

Первичные конечные точки

  • Primary Open Angle Glaucoma (POAG): Optic Nerve Evaluation [Срок оценки: Up to 5 years]
  • Age-Related Macular Degeneration (AMD): Dilated Macular Examination [Срок оценки: Up to 5 years]
  • Diabetic Retinopathy: Documentation of Presence or Absence of Macular Edema and Level of Severity of Retinopathy [Срок оценки: Up to 5 years]
  • Diabetic Retinopathy: Communication with the Physician Managing On-going Diabetes Care [Срок оценки: Up to 5 years]
  • Preventive Care and Screening: Influenza Immunization [Срок оценки: Up to 5 years]
  • Pneumonia Vaccination Status for Older Adults [Срок оценки: Up to 5 years]
  • Diabetes Mellitus: Dilated Eye Exam in Diabetic Patient [Срок оценки: Up to 5 years]
  • Documentation of Current Medications in the Medical Record [Срок оценки: Up to 5 years]
  • Melanoma: Continuity of Care - Recall System [Срок оценки: Up to 5 years]
  • Melanoma: Coordination of Care [Срок оценки: Up to 5 years]

Критерии участия

Критерии включения

  • Patients who meet the denominator requirements for each measure.

Критерии исключения

  • None

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

Здоровые добровольцы: Нет

Дизайн исследования

Модель наблюдения
Когортное

Центры проведения

США · 1 центр
  • American Academy of Opthalmology — San Francisco

Идентификаторы

NCT: NCT02485847 · IRIS Registry

Первоисточники (государственные реестры)

Открыть это исследование на ClinicalTrials.gov ↗