Overview
Corticosteroid Injection Combined With Cataract Surgery in Diabetic Eyes.
Status:
Completed
Completed
Trial end date:
2022-03-29
2022-03-29
Target enrollment:
0
0
Participant gender:
All
All
Summary
We aim in this study to investigate the effect of intravitreal triamcinolone acetonide injection on the development of macular edema and the progression of diabetic retinopathy. Whether this injection hastens cataract surgery results or not. We will categorize the participants into two groups: the case group who will receive the injection at the end of surgery, and the control group who will have routine cataract surgery with no extra injections.Phase:
Phase 2/Phase 3Accepts Healthy Volunteers?
NoDetails
Lead Sponsor:
Damascus UniversityTreatments:
Triamcinolone
Triamcinolone Acetonide
Triamcinolone diacetate
Triamcinolone hexacetonide
Criteria
Inclusion Criteria:- ● A history of diabetes mellitus DM type II that is well-confirmed by an
endocrinologist.
- Senile cataract that is causing visual disturbance as demonstrated by clinical
examination.
- CDVA of no more than 20/ 40, finger count and hand movement vision are included.
Too.
- Diabetic retinopathy that falls in one of the following categories according to
the International Clinical Diabetic Retinopathy Disease Severity Scale: No DR-
mild NPDR- moderate NPDR.
- A healthy-looking central macula, or Clinically Significant Macular Edema (CSME),
or edema that is apparent on Fundus Fluorescent Angiography (FFA) or OCT, as well
as a treatment-resistant diabetic macular edema in the past 24 months or
microaneurysms at foveal avascular zone (FAZ) borders not amenable to laser
therapy.
- Both sexes, Age 18 years or older.
- One eye per patient will be included.
- The surgery will be performed by the same surgeon and the samIOL design will be
used.
Exclusion Criteria:
- • A history of diabetes mellitus DM type I that is well-confirmed by an
endocrinologist or no history of DM.
- CDVA that is better than 20/40.
- functionally monocular patient as a result of moderate to severe visual
impairment in the contralateral eye, as per the definition of the International
Statistical Classification of Diseases and Related Health Problems, 10th revision
(6).
- The presence of pathologies other than diabetic retinopathy and cataract that may
justify visual acuity decline (e.g. corneal disease, age related macular
degeneration, macular hole, etc…).
- patients will be excluded if they had an increased risk for developing CME in the
study eye because of a complication during the current or previous intraocular
surgery, intraocular inflammation or uveitis, retinal vein occlusion, or macular
pathology that might influence visual function, other than diabetic macular
edema.
- Patients with pseudoexfoliation syndrome, Fuchs endothelial dystrophy, or
post-traumatic cataract in the study eye.
- Diabetic retinopathy that falls in one of the following categories according to
the International Clinical Diabetic Retinopathy Disease Severity Scale: severe
NPDR, proliferative DR, or vitreous hemorrhage requiring pan-retinal
photocoagulation or vitrectomy.
- Patients who used topical NSAIDs, topical or systemic corticosteroids before
surgery.
- patients who received an intravitreal injection with any kind of anti-VEGF in the
study eye in the previous 6 weeks, or an intraocular or periocular corticosteroid
injection in the previous 3 months.
- patients who received PRP during the past 3 months.
- Contraindications for any of the investigated drugs, particularly patients with
glaucoma, IOP of 21mm Hg or higher, previous steroid-induced IOP elevation, or
ganglion cell/ RNFL complex injury on OCT image.
- History of steroid hypersensitivity.
- Patients who are taking steroids PO with a total dosage of more than 5 mg/ day.
- Pregnant and breastfeeding ladies.
- Previous surgery on the study eye.
- systemic bleeding in the previous 3 months, major systemic surgery in the
previous 3 months, or a recent or recurrent cerebrovascular accident, myocardial
infarction, or thromboembolic event.