Event Group
Event Groups are part of the Adverse Events Module within the Results Section. They provide a way to organize and summarize adverse event data by grouping related events together.
Each Event Group typically represents a category or class of adverse events and includes statistical information such as the number of participants affected and at risk for different event types: deaths, serious events, and other events.
Event Group path is as follows:
Study -> Results Section -> Adverse Events Module -> Event Group
Event Group
Ignite Creation Date:
2025-12-25 @ 2:53 AM
Ignite Modification Date:
2025-12-26 @ 1:34 AM
NCT ID:
NCT05238233
Group ID:
EG000
Title:
Eye Dilation and Constriction
Description:
Participants screened for hyperopia \>+1 diopter using a phoropter, have their intraocular pressures measured using a tono pen, and have their iridocorneal angle measured with a gonio lens.
Proparacaine hydrochloride 0.5% eye drops will be used to numb the eyes before measuring intraocular pressures and prior to gonio lens.
The following day, the participant will receive one drop of tropicamide and one drop of 1% pilocarpine in the left eye.
If the left eye has no response to the 1% pilocarpine, or if the diameter of the pupil returned to baseline size, we will ask participants to come back to the clinic on another day to have the process repeated in the right eye.
Tropicamide: One drop will be given to participants
1% Pilocarpine: One drop will be given to participants
Proparacaine Hydrochloride: One drop will be given to participants
Tono pen AVIA: Participant intraocular pressures measured
VG4 Gonio: Participant iridocorneal angle measured
Reichert phoropter: Participant screened for hyperopia \>+1 diopter
Deaths Number Affected:
0
Deaths Number At Risk:
None
Serious Number Affected:
0
Serious Number At Risk:
10
Other Number Affected:
0
Other Number At Risk:
10
Study:
NCT05238233
Results Section:
NCT05238233
Adverse Events Module:
NCT05238233