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Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT02650050
Other study ID # GCO_2015_28
Secondary ID
Status Terminated
Phase N/A
First received
Last updated
Start date January 19, 2016
Est. completion date June 4, 2019

Study information

Verified date June 2019
Source Fondation Ophtalmologique Adolphe de Rothschild
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Diabetes is a major cause of blindness in adults in the developed countries. The retinal damages associated with diabetes lead to gradual loss of vision, which is accentuated when the macula is affected. This results in macular edema.

Currently, intravitreal injections of anti-VEGF have demonstrated their effectiveness and are the first line treatment of macular edema.

Subthreshold micropulsed laser photocoagulation is an alternative to conventional grid photocoagulation. By delivering pulsed impacts under the thermal lesion threshold of the pigment epithelium, it would not cause the side effects of conventional photocoagulation. Micropulsed photocoagulation combined to anti-VEGF injections, could be the most effective treatment with a minimum injection number and without epithelial lesions.

The main objective of this study is to show that the subthreshold micropulsed laser photocoagulation, in association with intravitreal injections of anti-VEGF, allows to reduce the number of anti-VEGF injections during the first year of treatment.

In this randomized, double blind study, eligible patients will be randomized between a micropulsed laser photocoagulation arm and a sham micropulsed laser photocoagulation arm.


Recruitment information / eligibility

Status Terminated
Enrollment 5
Est. completion date June 4, 2019
Est. primary completion date June 4, 2019
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- 18 years or more

- macular edema associated with a 1 or type 2 diabetes with a hemoglobin A1C level over 5.5% and under <13%

- indication for a treatment with intra-vitreal injections of ranibizumab

Exclusion Criteria:

- treatment with anti-VEGF during the previous 2 months

- treatment by intra-vitreous implant of dexamethasone during the previous six months

- previous history of vitrectomy or glaucoma

- photocoagulation during the previous 3 months

- patient's opposition to participate to the study

Study Design


Related Conditions & MeSH terms


Intervention

Radiation:
Micropulsed laser photocoagulation
Micropulsed laser photocoagulation after 3 anti-VEGF injections

Locations

Country Name City State
France Fondation ophtalmique Adolphe de Rothschild Paris

Sponsors (1)

Lead Sponsor Collaborator
Fondation Ophtalmologique Adolphe de Rothschild

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Number of intra-vitreal anti-VEGF injections One year
Secondary Time to reduction of the macular thickness One year
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