Retina Support Services, Inc
Tulsa, Oklahoma, 74127, United States
NCT Number: NCT00417703
This study will quantify the intraocular pressure elevation in the immediate time period following intravitreous injection. With more widespread use of intravitreous injections in patients that may require several injections per year, it is important to document the sudden increase in intraocular pressure, including the maximum intraocular pressure and the time required for the intraocular pressure to return to baseline. This data may be useful in stimulating additional studies to evaluate the long term ocular effects of repeated intravitreous injections.
We hypothesize that the intraocular pressure increases significantly following intravitreous injection and then returns to baseline during the initial thirty minutes following ranibizumab injection.
Looking for future studies?
Notify Me18 year and older
All sexes
Observational
Tulsa, Oklahoma, 74127, United States
We will assess the trend of intraocular pressure immediately following intravitreal injection of ranibizumab 0.5 mg (0.05 mL) by taking serial intraocular pressure readings every five minutes for thirty minutes after injection. This study is a prospective descriptive data collection consisting of measuring intraocular pressure immediately following intraocular injection, and at 5, 10, 15, 20, 25, and 30 minutes following injection of ranibizumab 0.5 mg.
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Oklahoma State University Center for Health Sciences
Other
A Prospective Investigation of the Intraocular Pressure Immediately Following Intravitreous Injection of Ranibizumab
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT02307682
Choroid Diseases, Choroidal Neovascularization
Fort Worth, Texas, United States
View Trial DetailsNCT02434328
Choroid Diseases, Choroidal Neovascularization
View Trial DetailsNCT00967850
Choroid Diseases, Choroidal Neovascularization
Santiago de Compostela, La Coruña, Spain
View Trial DetailsNCT05662943
Age-Related Macular Degeneration, Choroid Diseases
Seoul, South Korea
View Trial Details