- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05332665
AS-OCT Evaluation of Iridocorneal Angle of Patients of Angle Closure Glaucoma After Phacoemulsification
Anterior Segment Optical Coherence Tomography Evaluation of Iridocorneal Angle of Patients of Angle Closure Glaucoma After Phacoemulsification and YAG Laser Iridotomy, Comparative Study
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
The recent treatment of ACG is phacoemulsification in patients of acute attack with YAG laser iridotomy in the other eye.
The AS-OCT will be used for evaluation of the angle of the anterior chamber parameters in both eyes after phacoemulsification and YAG laser peripheral iridotomy.
Follow up of AS-OCT will be done 1,3,6 months after surgery and we will compare results in each eye and between both eyes.
.
Study Type
Enrollment (Anticipated)
Contacts and Locations
Study Contact
- Name: mohamed Salah
- Phone Number: 01003321802
- Email: drmsalah1982@yahoo.com
Study Locations
-
-
El Minia
-
Minia, El Minia, Egypt, 61111
- Recruiting
- Mohamed Mahmoud
-
Contact:
- mohamed Mahmoud
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- patients with acute attack of angle closure glaucoma in one eye.
- Patients fit for phacoemulsification
Exclusion Criteria:
- 1- Patients with history of any intraocular surgery. 2- Patients with history of refractive surgery. 3- Patients with diabetic retinal vasculopathy or retinal detachment. 4- Patients with chronic angle closure glaucoma, open angle glaucoma or 2ry glaucoma
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Angle opening distance (AOD)
The AOD measured as perpendicular distance between anterior iris surface and point at trabecular meshwork at 500 μm anterior to the scleral spur
|
Anterior segment optical coherence tomography (AS OCT) is an imaging device that can acquire an anterior segment image using a noncontact method with the patient in a sitting position.
This device provides reproducible and quantitative measurements of the AC angle and other anterior segment parameters.
medical procedure which uses a laser device to create a hole in the iris, thereby allowing aqueous humor to traverse directly from the posterior to the anterior chamber and, consequently, relieve a pupillary block
|
|
Trabecular iris space area (TISA) 500
TISA 500 was measured as an area bounded anteriorly by the AOD 500, posteriorly by a line drawn from the scleral spur perpendicular to the plane of the inner scleral wall to the opposing iris, superiorly by the inner corneoscleral wall, and inferiorly by the iris surface
|
Anterior segment optical coherence tomography (AS OCT) is an imaging device that can acquire an anterior segment image using a noncontact method with the patient in a sitting position.
This device provides reproducible and quantitative measurements of the AC angle and other anterior segment parameters.
medical procedure which uses a laser device to create a hole in the iris, thereby allowing aqueous humor to traverse directly from the posterior to the anterior chamber and, consequently, relieve a pupillary block
|
|
Anterior chamber depth (ACD)
The ACD was measured as the perpendicular distance from the corneal endothelium at the corneal apex to the anterior lens surface
|
Anterior segment optical coherence tomography (AS OCT) is an imaging device that can acquire an anterior segment image using a noncontact method with the patient in a sitting position.
This device provides reproducible and quantitative measurements of the AC angle and other anterior segment parameters.
medical procedure which uses a laser device to create a hole in the iris, thereby allowing aqueous humor to traverse directly from the posterior to the anterior chamber and, consequently, relieve a pupillary block
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
IOP
Time Frame: up to 6 months
|
mmhg
|
up to 6 months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Corneal endothelial count
Time Frame: up to 6 months
|
CD per mm2
|
up to 6 months
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: mohamed Salah, Minia faculty of medicine
Study record dates
Study Major Dates
Study Start (ACTUAL)
Primary Completion (ANTICIPATED)
Study Completion (ANTICIPATED)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (ACTUAL)
Study Record Updates
Last Update Posted (ACTUAL)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- AS-OCT in ACG
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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