Multifocal Chromatic Pupilloperimetry in Patients With Pseudotumor Cerebri and Healthy Subjects.
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: objective chromatic multifocal pupillometer.
- Кому может быть актуально
- Состояния в реестре: Pseudotumor Cerebri. Базовые параметры: 18 лет — 80 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
- Израиль
- 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
Assessment of Pupillary Response and Visual Field Defects by Objective Multifocal Chromatic Pupillometer in Patients With Pseudotumor Cerebri and Healthy Subjects
Обзор
PTC(Pseudotumor cerebri) patients may develop increased Intracranial pressure (ICP) that can produces increased pressure around the distal optic nerve,which is likely followed by venule compression, ischemia, and loss of visual function.Vision loss in PTC is most commonly characterized by standard automated perimetry to measure peripheral visual field sensitivity. Pupillometry is a promising approach for functional assessment in PTC because it is noninvasive, objective, performed quickly with minimal patient cooperation needed. The feasibility of using chromatic multifocal pupillometry for assesment of PTC will be examined.
Вмешательства
- Диагностический тест objective chromatic multifocal pupillometer
objective chromatic multifocal pupillometer (OCMP) enables objective and accurate measurement of pupillary responses to chromatic light at different wavelengths and light intensities and at different visual field locations.
Первичные конечные точки
- Measurement of maximal precentage of pupil contraction and dilation in response to chromatic light stimulus [Срок оценки: single visit: 1 day]
- Measurement of maximal velocity of pupil contraction and dilation in response to chromatic light stimulus [Срок оценки: single visit: 1 day]
- Measurement of latency of pupil contraction and dilation in response to chromatic light stimulus [Срок оценки: single visit: 1 day]
Вторичные конечные точки (11)
- Subjective visual field [Срок оценки: single visit: 1 day]
- Optic nerve structure by OCT [Срок оценки: single visit: 1 day]
- Change from baseline pupil contraction and dilation precentage in PCT patients at 48 hours [Срок оценки: single visit: 1 day, 48 hours after baseline testing]
- Change from baseline pupil contraction and dilation maximal velocity in PCT patients at 48 hours [Срок оценки: single visit: 1 day, 48 hours after baseline testing]
- Change from baseline pupil contraction and dilation latency in PCT patients at 48 hours [Срок оценки: single visit: 1 day, 48 hours after baseline testing]
- Change from baseline pupil contraction and dilation precentage in PCT patients at 1 week. [Срок оценки: single visit: 1 day, 1 week after baseline testing]
- Change from baseline pupil contraction and dilation maximal velocity in PCT patients at 1 week. [Срок оценки: single visit: 1 day, 1 week after baseline testing]
- Change from baseline pupil contraction and dilation latency in PCT patients at 1 week. [Срок оценки: single visit: 1 day, 1 week after baseline testing]
- Change from baseline pupil contraction and dilation precentage in PCT patients at 2 months. [Срок оценки: single visit: 1 day, 2 months after baseline testing]
- Change from baseline pupil contraction and dilation maximal velocity in PCT patients at 2 months. [Срок оценки: single visit: 1 day, 2 months after baseline testing]
- Change from baseline pupil contraction and dilation latency in PCT patients at 2 months. [Срок оценки: single visit: 1 day, 2 months after baseline testing]
Критерии участия
Критерии включения
Healthy subjects
- Male or female patients, age between 18 and 80 years, inclusive
- Informed written consent will be obtained from all participants.
- Normal eye examination
- Best-corrected visual acuity (BCVA) of 20/20
- Normal color vision test (Ishihara/HRR)
- Normal Spectral-Domain Optical Coherence Tomography (SD-OCT)
- Normal 24-2 Humphrey visual field (SITA Standard) and:
- Short duration (≤10 minutes)
- Minimal fixation losses, False POS errors and False NEG errors (less than 33% for each one of reliability indices)
PTC patients
- Male or female patients, age between 18 and 80 years, inclusive
- Best-corrected visual acuity (BCVA) of at least 20/100 in worse eye
- Optic disc edema
- PTC diagnosis based on Modified Dandy Criteria ( lumbar puncture with opening pressure higher than or equal to 25 cm H2O, normal cerebrospinal fluid constituents, and unremarkable brain imaging results except typical for PTC
Критерии исключения
Healthy subjects
- History of past (last 3 months) or present ocular disease or ocular surgery
- Use of any topical or systemic medications that could adversely influence pupillary reflex
- Intolerance to gonioscopy, slit lamp examination, Goldmann applanation tonometry or other schedule study procedure.
- Mental impairment or instability such as that informed consent may not be obtained or compliance with tester instructions is unlikely.
- Visual media opacity including cloudy corneas.
- Any condition preventing accurate measurement or examination of the pupil.
PTC patients
- Any other neurologic or ophthalmic disease other than PTC
- Use of any topical or systemic medications that could adversely influence pupillary reflex
- Intolerance to gonioscopy, slit lamp examination, Goldmann applanation tonometry or other schedule study procedure.
- Mental impairment or instability such as that informed consent may not be obtained or compliance with tester instructions is unlikely.
- Visual media opacity including cloudy corneas.
- Any condition preventing accurate measurement or examination of the pupil.
Критерии приведены из реестра в оригинале (на английском). Окончательную оценку соответствия проводит исследовательский центр.
Здоровые добровольцы: Да
Дизайн исследования
- Распределение
- Нерандомизированное
- Модель
- Параллельные группы
- Маскирование
- Открытое
- Основная цель
- Диагностика
Центры проведения
Израиль · 1 центр
- Sheba Medical Center — Tel Litwinsky
Идентификаторы
NCT: NCT03304314 · SHEBA-17-3754-YR-CTIL