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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01358396
Other study ID # HB-DME-1
Secondary ID
Status Completed
Phase Phase 1
First received May 19, 2011
Last updated May 20, 2011
Start date January 2010
Est. completion date October 2010

Study information

Verified date January 2010
Source Cairo University
Contact n/a
Is FDA regulated No
Health authority EGYPT:Faculty of Medicine, Research Committee,Cairo University
Study type Observational

Clinical Trial Summary

Does diabetic patients' glycemic control affect their response to laser and/or intravitreal injection therapy in terms of visual and anatomical outcomes.


Description:

To evaluate the visual and anatomical response to therapy in patients with diabetic macular edema (DME) in relation to their glycemic control.

Patients with DME with central foveal thickness (CFT) > 250µm with no proliferative disease had their glycosolated hemoglobin (HbA1c) measured at baseline and 3 months. CFT by optical coherence tomography, and best corrected visual acuity (BCVA) in logMARs were measured at baseline, 1, and 3 months. Exclusion criteria: laser or intravitreal injections within 6 months, hard exudates within 500um of the foveal center, or macular traction. Therapy included laser and intravitreal anti VEGFs. HbA1c graded as: G1=<7%, G2= 7-7.9%, G3= 8-8.9%, G4 = >9%; and as: low <8%, high ≥ 8%.


Recruitment information / eligibility

Status Completed
Enrollment 52
Est. completion date October 2010
Est. primary completion date July 2010
Accepts healthy volunteers No
Gender Both
Age group 20 Years to 80 Years
Eligibility Inclusion Criteria:

- Central foveal thickness more than 250 microns

Exclusion Criteria:

- Proliferative Diabetic Retinopathy.

- Traction Macular Membranes

- Previous Laser or intravitreal injections within 6 months.

Study Design

Observational Model: Cohort, Time Perspective: Prospective


Related Conditions & MeSH terms


Intervention

Other:
Respond to therapy for diabetic macular edema
Correlate HBA1c with visual acuity outcome to therapy.

Locations

Country Name City State
Egypt Cairo University Cairo

Sponsors (1)

Lead Sponsor Collaborator
Cairo University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary Visual Acuity Correlate baseline HBA1c to the visual outcomes. 3 months No
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