Ignite Creation Date:
2024-05-06 @ 5:13 PM
Last Modification Date:
2024-10-26 @ 2:24 PM
Study NCT ID:
NCT05238233
Status:
COMPLETED
Last Update Posted:
2023-03-07
First Post:
2022-02-03
Brief Title:
Wearing-Off Period of Pharmacological Dilation and Anisocoria
Sponsor:
Prisma Health-Upstate
Organization:
Prisma Health-Upstate
Study Overview
Official Title:
The Wearing-Off Period of Pharmacological Dilation An Addendum to the Management of Anisocoria
Status:
COMPLETED
Status Verified Date:
2023-01
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
Students at the School of Medicine Greenville will be asked to participate in this study
The aim of this study is to better understand when medical imaging is needed for patients with anisocoria unequal pupil size
Participation in the study includes up to 3 visits over a period of one week Each study visit will last about 30 minutes
At the first visit participants will be screened for hyperopia using a phoropter have their intraocular pressures taken using a tono-pen and have their iridocorneal angle measured using gonioscopy at the ophthalmology clinic Proparacaine hydrochloride 05 eye drops will be used to numb the eyes before measuring intraocular pressures and prior to gonio lens exam Participants will also be asked to complete three forms
Participants will be asked to return to the clinic on a scheduled day within one week of the screening visit to have their left eye dilated At this visit the diameter of the pupil will be measured using a Near card in a windowless room with a set light-level Then the participant will receive one drop of tropicamide in the left eye After the drops have had time to take effect which will be about 20-30 minutes later the diameter of the pupil will be measured again
Participants will then be asked to return to the clinic in 3-4 hours At this time the diameter of the pupil will be measured again
The third type of eye drop used in this study is 1 pilocarpine 1 pilocarpine will briefly constrict the eyes One drop of 1 pilocarpine will be administered to left eye and the change in pupillary diameter will be measured if any It will take about 10-15 minutes for the 1 pilocarpine to take effect
Participants may be required to attend 2 additional 30-minute visits on a third day depending on how their eyes respond to the drops
This study will recruit about 10-15 participants
The aim of this study is to better understand when medical imaging is needed for patients with anisocoria unequal pupil size
Participation in the study includes up to 3 visits over a period of one week Each study visit will last about 30 minutes
At the first visit participants will be screened for hyperopia using a phoropter have their intraocular pressures taken using a tono-pen and have their iridocorneal angle measured using gonioscopy at the ophthalmology clinic Proparacaine hydrochloride 05 eye drops will be used to numb the eyes before measuring intraocular pressures and prior to gonio lens exam Participants will also be asked to complete three forms
Participants will be asked to return to the clinic on a scheduled day within one week of the screening visit to have their left eye dilated At this visit the diameter of the pupil will be measured using a Near card in a windowless room with a set light-level Then the participant will receive one drop of tropicamide in the left eye After the drops have had time to take effect which will be about 20-30 minutes later the diameter of the pupil will be measured again
Participants will then be asked to return to the clinic in 3-4 hours At this time the diameter of the pupil will be measured again
The third type of eye drop used in this study is 1 pilocarpine 1 pilocarpine will briefly constrict the eyes One drop of 1 pilocarpine will be administered to left eye and the change in pupillary diameter will be measured if any It will take about 10-15 minutes for the 1 pilocarpine to take effect
Participants may be required to attend 2 additional 30-minute visits on a third day depending on how their eyes respond to the drops
This study will recruit about 10-15 participants
Detailed Description:
None
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
True
Is a FDA Regulated Device?:
True
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
True
Is an FDA AA801 Violation?:
None