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NCT00802269 Clinical Trial

Pain Using Reduced Fluence Parameters in Photocoagulation for Diabetic Retinopathy.

Proliferative Diabetic Retinopathy Clinical Trial

Official title:
Pain Using Reduced Fluence Parameters in Photocoagulation for Diabetic Retinopathy.

Clinical Trial Details — Status: Terminated

Administrative data
NCT number NCT00802269
Other study ID # APEC-032
Secondary ID
Status Terminated
Phase Phase 4
First received
Last updated
Start date March 2008
Est. completion date November 2008

Study information
Verified date May 2024
Source Asociación para Evitar la Ceguera en México
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The used of reduced fluence parameters for panretinal photocoagulation decreases pain as perceived by the patient, compared to traditional parameters.

Recruitment information / eligibility
Status Terminated
Enrollment 25
Est. completion date November 2008
Est. primary completion date November 2008
Accepts healthy volunteers No
Gender All
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria: - Patients 18 years or older, that signed informed consent - Proliferative diabetic retinopathy with indication for panretinal photocoagulation Exclusion Criteria: - Previous retinal photocoagulation - Previous ocular surgical procedures - Ocular media opacities - History of trigeminal neuralgia - Chronic ocular pain - Depression under conductual or medical treatment

Study Design

Related Conditions & MeSH terms

Intervention

Procedure:
• Retinal laser photocoagulation
Retinal laser photocoagulation using a 532 nm laser

Locations
Country Name City State
Mexico Asociacion para Evitar la Ceguera en Mexico Mexico City DF

Sponsors (1)
Lead Sponsor Collaborator
Asociación para Evitar la Ceguera en México

Country where clinical trial is conducted

Mexico, 

Outcome
Type Measure Description Time frame Safety issue
Primary Pain (NRS-11 scale) Immediately post-treatment
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