- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02555956
Grid Laser for Diffuse Diabetic Maculopathy (MMG)
September 20, 2015 updated by: Jamshed Ahmed, Dow University of Health Sciences
Subthreshold Double Frequency Nd. YAG Grid Laser for Diffuse Diabetic Maculopathy
Diabetic related complications are increasing day by day due to increse in the number of diabetic patients all over the world.
Diabetic macular edema is one of them and a major cause of vision imparment.
Various kind of treatment modalities are preent to treat this coplication.
Grid laser is one treatment modality.
Laser phtocoagulation is a destrictive procedure.Laser power if kept to aminimum can get the desired results without severe destruction to the retina .
In this study, the investigators are going to document the effect of minimal grid laser tn loss o overcome the visioe to diabetic macular edema.
Study Overview
Status
Completed
Conditions
Study Type
Observational
Enrollment (Actual)
50
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Sindh
-
Karachi, Sindh, Pakistan, 75500
- Dow universty Hospital,Dow international Medical college
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
20 years to 80 years (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
Diabetic patients having diffuse diabetic macular edema.
Description
Inclusion Criteria:
- Diabetic patients with macular edema.
- both sexes
- conset to participate.
Exclusion Criteria:
- focal edema.
- patients requiring only the focal laser.
- patients with proferative diabetic retinopathy.
- Patients with ischaemic maculopathy on fundus fluorescein angiography.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Improvement of visual acuity after grid laser
Time Frame: 6 week
|
Visual acuity will be mesured pre laser and 06 weeks post laser
|
6 week
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Complication
Time Frame: during first six weeks after laser
|
Patiens willbe asked and examined for any potentiail anticipated complication.
|
during first six weeks after laser
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: Dr. Jamshed Ahmed, FCPS, Dow university of health sciences, karachi
- Principal Investigator: Jamshed Ahmed, FCPS, Dow University of Health Sciences
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
April 1, 2012
Primary Completion (Actual)
December 1, 2014
Study Completion (Actual)
December 1, 2014
Study Registration Dates
First Submitted
August 6, 2015
First Submitted That Met QC Criteria
September 20, 2015
First Posted (Estimate)
September 22, 2015
Study Record Updates
Last Update Posted (Estimate)
September 22, 2015
Last Update Submitted That Met QC Criteria
September 20, 2015
Last Verified
September 1, 2015
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- Macular Grid Laser
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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