The Effect of Glaucoma Drops on of the Duration of a Pure Intraocular Gas Bubble
Completed · Not applicable
Conditions studied: Scleral Buckling
In brief
A controlled clinical study comparing the effect of topical aqueous suppressants on intraocular gas duration.
Key facts
- Study ID
- NCT01843920
- Run by
- Jason Hsu, MD
- People needed
- 21
- Starts
- 2011-06-01
- Expected to finish
- 2013-04-01
- Last updated by the study team
- 2018-05-30
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Ability to provide written informed consent and comply with study assessments for the full duration of the study.
- Have undergone eye surgery including scleral buckling or pneumatic retinopexy for treatment of retinal detachment other condition at the discretion of the investigator.
You may not qualify if…
- Prior surgery to treat glaucoma.
- Current use of glaucoma eye drops.
- Absence of a lens in the eye or presence of a lens implant in front of the iris (colored part of your eye).
- Allergy or contraindication to any of the glaucoma drops being used in this study (e.g., sulfa allergy, asthma, chronic obstructive pulmonary disease (bronchitis or emphysema), slow heart rate).
Where it is running
- Mid Atlantic Retina- Wills Eye Institute — Philadelphia, Pennsylvania, United States
Full record on ClinicalTrials.gov
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