Triamcinolone Acetonide in Patients With Serous Pigment Epithelial Detachment
NCT04292756 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 63
Last updated 2022-08-23
Summary
The purpose of this study is to determine the effectiveness and safety of triamcinolone acetonide in patients with serous pigment detachment associated with age-related macular degeneration
Conditions
- Age-Related Macular Degeneration
Interventions
- PROCEDURE
-
Subtenon injection of 40 mg triamcinolone acetonide
Subtenon injection of 40 mg triamcinolone acetonide: 1 initial injection of 40 mg triamcinolone acetonide, further injections will be base at month 3 examination.
- PROCEDURE
-
Intravitreal injection of 4 mg triamcinolone acetonide
Intravitreal injection of 4 mg triamcinolone acetonide: 1 initial injection of 4 mg triamcinolone acetonide, further injections will be base at month 3 examination.
- DIAGNOSTIC_TEST
-
Visometry
Ophthalmic examination
- DIAGNOSTIC_TEST
-
Fluorescent angiography
Ophthalmic examination
- DIAGNOSTIC_TEST
-
Refractometry
Ophthalmic examination
- DIAGNOSTIC_TEST
-
Slit lamp examination
Ophthalmic examination
- DIAGNOSTIC_TEST
-
Ophthalmoscopy
Ophthalmic examination
- DIAGNOSTIC_TEST
-
OKT
Ophthalmic examination
- DIAGNOSTIC_TEST
-
IOP
Ophthalmic examination
Sponsors & Collaborators
-
Odessa National Medical University
collaborator OTHER -
Mykolaiv Region Ophthalmogical Hospital
collaborator OTHER -
Central Polyclinic of Internal Affairs of Ukraine
collaborator OTHER_GOV -
The Filatov Institute of Eye Diseases and Tissue Therapy
lead OTHER
Principal Investigators
-
Andrii MD Korol, PhD · The Filatov Institute of Eye Diseases and Tissue Therapy
Study Design
- Allocation
- RANDOMIZED
- Purpose
- TREATMENT
- Masking
- NONE
- Model
- PARALLEL
Eligibility
- Min Age
- 50 Years
- Max Age
- 90 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2018-03-27
- Primary Completion
- 2020-07-01
- Completion
- 2020-12-31
Countries
- Ukraine
Study Locations
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