Triamcinolone Acetonide in Patients With Serous Pigment Epithelial Detachment

NCT04292756 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 63

Last updated 2022-08-23

No results posted yet for this study

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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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04292756 on ClinicalTrials.gov