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OpenTrials
Completed

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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Key information

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

Vitreous Tamponade with Silicone Oil

Device

Primary outcomes

  1. 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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