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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04285151
Other study ID # TUOR002
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date January 2015
Est. completion date January 2020

Study information

Verified date February 2020
Source Tanta University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Premacular Subhyaloid hemorrhage is a sudden profound loss of vision in eyes with proliferative diabetic retinopathy (PDR). Pars plana vitrectomy is the treatment of choice for premacular hemorrhage in eyes with proliferative changes. Nd:YAG laser hyaloidotomy has been used to evacuate the premacular hemorrhage


Recruitment information / eligibility

Status Completed
Enrollment 25
Est. completion date January 2020
Est. primary completion date January 2020
Accepts healthy volunteers No
Gender All
Age group 21 Years to 60 Years
Eligibility Inclusion Criteria:

- Eyes with premacular subhyaloid hemorrhage of more than 3 disc diameters, involving the fovea.

- Eyes with proliferative diabetic retinopathy

Exclusion Criteria:

- Dense media opacity (corneal/cataract)

- Patients with bleeding tendency or on anti-coagulant drugs

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Nd:YAG laser Hyaloidotomy
Using the YAG laser for opening the posterior hyaloid in eyes with premacular hemorrhage, and evacuating the entrapped hemorrhage

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Tanta University

Outcome

Type Measure Description Time frame Safety issue
Primary Visual acuity improvement Testing VA after YAG laser 1 week
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