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Micropulse 810 Nanomolar (nm), Diode Laser for Diffuse Diabetic Macular Edema

Information source: Federal University of São Paulo
Information obtained from ClinicalTrials.gov on November 03, 2008
Link to the current ClinicalTrials.gov record.

Condition(s) targeted: Diabetic Macular Edema

Intervention: Laser photocoagulation (Device)

Phase: Phase 2

Status: Recruiting

Sponsored by: Federal University of São Paulo

Official(s) and/or principal investigator(s):
Jose A Cardillo, Principal Investigator, Affiliation: Federal University of Sao Paulo- Department of Ophthalmology

Overall contact:
Daniel Lavinsky, Phone: 55-11-7658-8669, Email: lavinsky@via-rs.net

Summary

Objective: To compare micropulse 810nm diode laser photocoagulation versus argon laser photocoagulation for treatment of diabetic macular edema. Micropulse laser technique will be determined by an initial clinical trial comparing single versus double density laser photocoagulation techniques for treatment of diabetic macular edema. The single density is based on the Early Treatment Diabetic Retinopathy Study (ETDRS) grid photocoagulation technique and the double density increases the number of spots.

Methods: Patients with diabetic macular edema will be assigned to receive either micropulse 810nm diode laser photocoagulation or argon laser photocoagulation therapy. First, in a smaller clinical trial, patients will be assigned to single or double density micropulse 810nm diode laser to determine best strategy for this therapy. Visual acuity, fundus photographs and fluorescein angiography, and optical coherence tomography measurements , autofluorescence and mfERG were obtained at baseline and at 1, 3 and 6 months and 12 months.

Clinical Details

Official title: Phase 2 Study of Micropulse 810nm Diode Laser Photocoagulation for Treatment of Diffuse Diabetic Macular Edema

Study design: Treatment, Randomized, Single Blind (Subject), Active Control, Parallel Assignment

Primary outcome: Macular thickness measured by optical coherence tomography (OCT)

Secondary outcome:

Safety profile

Selectivity of laser therapy (autofluorescence and mfERG)

Eligibility

Minimum age: 18 Years. Maximum age: N/A. Gender(s): Both.

Criteria:

Inclusion Criteria:

- Diabetes mellitus (type 1 or 2)

- Diabetic macular edema in study eye associated to diabetic retinopathy

- Diffuse macular edema defined as macular thickening determined by biomicroscopy and

fluorescein angiography.

- Best corrected visual acuity between 34 (20/200) and 68 letters (20/50).

- Macular thickness greater than 300 mcm on OCT.

Exclusion Criteria:

- Uncontrolled systemic disease

- Start of medical therapy for diabetes or change in treatment from oral to insulin four

months before initial visit.

- HbA1c levels greater than 10%

- Presence of retinal venous occlusion, cystoid macular edema,or other condition that

would contribute to macular edema.

- Presence of epiretinal membrane

- Presence of vitreomacular traction in the study eye.

- Neovascularization of disc or elsewhere in the study eye.

- History or presence of choroidal neovascularization in the study eye.

- Presence of rubeosis irides in the study eye.

- Eye opacity that interfere with clinical documentation and photography.

- Intra-ocular surgery 90 days before initial visit.

- Scheduled surgery for study eye.

- Patients with known allergies to fluorescein.

Locations and Contacts

Daniel Lavinsky, Phone: 55-11-7658-8669, Email: lavinsky@via-rs.net

Vision Institute, Federal University of Sao Paulo, Sao Paulo, SP, Brazil; Recruiting
Daniel Lavinsky, MD, Phone: 55-11-7658-8669
Jose A Cardillo, Principal Investigator
Michel E Farah, Principal Investigator
Paulo Hilarião, Sub-Investigator
Leonardo Castro, Sub-Investigator
Daniel Lavinsky, Sub-Investigator
Additional Information

Starting date: March 2007
Ending date: November 2008
Last updated: May 6, 2008

Page last updated: November 03, 2008

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