Effect of Ambient Light on the Parameters of the Pupillary Light Reflex
- Conditions
- Healthy Volunteers
- Interventions
- Other: Pupillometry
- Registration Number
- NCT01207817
- Brief Summary
The purpose of this study is to determine the effects of varying luminescent levels on the pupillary response.
- Detailed Description
Evaluation of the pupillary response is an underemphasized aspect of the assessment of visual function. The pupillary light reflex is one of the few objective indicators of afferent input from the retina and optic nerve. Since the pupillary light reflex is processed through the retina, it may be used to assess visual integrity (1). Pupillometry is a reliable technology capable of providing repetitive data on quantitative pupillary function in states of health and disease (2). Amplitude, latency, maximum constriction velocity, mean constriction velocity, and dilation velocity are measured using the Neuroleptics pupillometer. The effects of varying levels of ambient light on these parameters of the pupillary response have not been extensively studied. The purpose of this investigation is to determine the effects of varying luminescent levels on the pupillary response.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 30
- healthy volunteers
- recent bout of conjunctivitis or infection in the eye recent eye surgery seizure disorder unable to lie flat for 30 minutes known history of eye disease which cannot be corrected with lenses
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Arm && Interventions
Group Intervention Description no condition Pupillometry no condition - healthy volunteers
- Primary Outcome Measures
Name Time Method pupillary light reflex: amplitude, latency, maximum constriction velocity, mean constriction velocity and dilation velocity during different levels of ambient light Pupillometry readings will be taken at 3 potential light readings low light, intermediate light and high ambient light. A total of 48 readings will be done. All parameters will be done at one sitting and will take approximately 45 minutes to complete.
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
UMDNJ-University Hospital
🇺🇸Newark, New Jersey, United States