Retinal Ischemia in Central Retinal Vein Occlusion, and the Effects of Treatment With Intravitreal Ranibizumab

Central Retinal Vein Occlusion Clinical Trial

— LuRVO  

Official title:

Objective Measurement of Retinal Ischemia in Central Retinal Vein Occlusion, and the Effects of Treatment With a Vascular Endothelial Growth Factor Inhibitor.

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01360385
• Other study ID #: LuRVO
• Status: Completed
• Phase: N/A
• First received: October 28, 2010
• Last updated: September 11, 2012
• Start date: October 2010
• Est. completion date: July 2012

Study information

• Verified date: September 2012
• Source: Glostrup University Hospital, Copenhagen
• Contact: n/a
• Is FDA regulated: No
• Health authority: Denmark: The Regional Committee on Biomedical Research Ethics
• Study type: Observational

Clinical Trial Summary

Recent studies have shown a remarkably positive effect of 6 monthly injections of Ranibizumab on eyes with CRVO. The disease may cause severe sight threatening complications, partly due to restrictions in blood flow and oxygenation . Although Ranibizumab has been shown affective to reduce oedema of the retina, it is not known whether the drug ameliorates or aggravates restrictions in oxygenation.

The Oxymap oximeter allows a non-invasive measurement of the oxygen saturation in retinal vessels and thus the state of retinal oxygenation.

The primary objective of the study is to evaluate the effects of injections of Ranibizumab on the retinal oxygen saturation in eyes with newly diagnosed central retinal vein occlusion (CRVO),

The secondary objective is to evaluate the effects of injections of Ranibizumab on visual acuity and retinal oedema in eyes with different degree of ischemia.

Description:

Background and objectives

The CRUISE study has shown a remarkable positive effect of 6 monthly injections intravitreal Ranibizumab on visual function in eyes with macular edema secondary to CRVO. Eyes with CRVO are at risk of severe complications to retinal ischemia, particularly proliferative retinopathy and neovascular glaucoma. It is not known whether intravitreal anti-VEGF therapy ameliorates or aggravates retinal ischemia and thus the risk of ischemic complications is unknown. Since complications to retinal ischemia take time to develop, and are relatively infrequent, the CRUISE study was not designed, or powered, to investigate the impact of intravitreal anti-VEGF treatment on these complications.

The Oxymap oximeter allows objective non-invasive measurement of the oxygen saturation in retinal vessels and thus the degree of retinal ischemia. The rationale behind the present study is to use this instrument in order to obtain preliminary information on the effects of intravitreal anti-VEGF treatment on retinal ischemia in CRVO eyes without having to wait for ischemic complications to arise in a large study population.

The primary objective of the study is to evaluate the effects of treatment with intravitreal Ranibizumab on the retinal oxygen saturation in eyes with newly diagnosed central retinal vein occlusion (CRVO),

The secondary objective is to evaluate the effects of intravitreal Ranibizumab on visual acuity and central retinal thickness in eyes with different degree of ischemia.

Study design

The research project is a case-series study of CRVO-patients with three monthly injections of Ranibizumab and a 3 month follow-up period, during which Ranibizumab injections are provided as needed.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 24
• Est. completion date: July 2012
• Est. primary completion date: July 2012
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

1. Central retinal vein occlusion in one eye.

2. Planned treatment with intravitreal injections of Lucentis (ranibizumab)

3. Functional fellow eye.

Exclusion Criteria:

1. Current or previous medical condition that in the opinion of the investigator may confound assessment of study results or put where the study methods may put the patient at risk.

2. Patients who are unable to receive treatment with vascular endothelial growth factor inhibitors.

3. Prior panretinal photocoagulation in the study eye.

4. Prior intraocular surgery in the study eye, other than cataract operation.

5. Any intravitreal injection 6 months prior to study baseline

6. Participation in another clinical study that, in the opinion of the investigator, may confound the assessment of study results.

Study Design

Observational Model: Case-Only, Time Perspective: Prospective

Related Conditions & MeSH terms

• Central Retinal Vein Occlusion
• Retinal Vein Occlusion

Locations

Country	Name	City	State
Denmark	Department of Ophthalmology, Glostrup Hospital	Copenhagen	Glostrup

Sponsors (2)

Lead Sponsor	Collaborator
Glostrup University Hospital, Copenhagen	Novartis

Country where clinical trial is conducted

Denmark, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Retinal oxygen saturation	Oxygen saturation is measured with the Oxymap Retinal Oximeter, which allows for objective, non-invase oximetry in retinal vessel.; The outcome measure will be the change in saturation from baseline to 6 months after first injection.	6 months after first injection of ranibizumab.	No
Secondary	Visual acuity	Visual acuity measured by the ETDRS standard at 4 meters, 2 meters and 1 meter, where applicable.; The outcome measure will be the mean change in visual acuity, measured in ETDRS letters, from baseline to 6 months after first injection.	6 months after first injection of ranibizumab.	No
Secondary	Central retinal thickness	Central retinal thickness as measured with optical coherence tomography.; The outcome measure will be the mean change in central retinal thickness, from baseline to 6 months after first injection.	6 months after first injection of ranibizumab.	No