NCT Number: NCT02675543
Vitreous Inflammation in Standard and Heavy Silicone Oil
The inflammatory response after prolonged retinal detachment and after vitreoretinal surgery has its apex in the development of PVR that occurs when retinal cells are exposed to the inflammatory milieu in the humor vitreous.
This situation is common in complicated retinal detachment, but is amplified after invasive surgery and by the use of intraocular tamponades that float over a subtle film of liquid where the inflammatory cytokines and growth factors reach the critical concentration over the inferior retina.
Many authors have noted that the heavy tamponade are more prone to cause intraocular inflammation compared to standard silicone oil, especially if they remain for several months in the eye.
The purpose of this study is to measure the vitreous concentration of some of the most important cytokines involved in the inflammatory vitreal response.
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Notify MeKey information
Conditions
Age range
18 year and older
Sex eligibility
All sexes
Study type
Interventional
Phase
Not applicable
Who can participate
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
- patient scheduled for vitrectomy
Exclusion criteria
- diabetic retinopathy
- uveitis
Treatment and study plan
Primary outcomes
-
Vitreous Prostaglandin E2 Levels
Time frame: intraoperarive
Sponsors and collaborators
Lead sponsor
Università degli Studi di Brescia
Other
Registry information
Important dates
- Study start
- 2015
- Primary completion
- 2015
- First posted
- Feb 5, 2016
- Registry last updated
- Jun 2, 2017
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.
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