Suprachoroidal Triamcinolone for Macular Edema in Resistant Non-Infectious Uveitis
Suprachoroidal triamcinolone acetonide injection
Eye Diseases+2
+ Macular Degeneration
+ Macular Edema
Treatment Study
Summary
Study start date: September 1, 2024
Actual date on which the first participant was enrolled.This study investigates a new treatment option for people with a specific type of eye inflammation, known as non-infectious uveitis, which leads to swelling in the central part of the retina (called macular edema). The swelling can threaten vision and is particularly challenging to treat in patients who haven't responded to the usual steroid injections around the eye. The study aims to determine if injecting a medicine called triamcinolone directly into a part of the eye called the suprachoroidal space can help reduce the swelling and improve vision. This approach could provide a new treatment possibility for those who haven't found relief with existing methods. Participants in the study will first undergo an assessment that includes a vision test and an eye examination involving a special scan called OCT to evaluate the retina. They will then receive a single injection of triamcinolone into the suprachoroidal space of the eye. This procedure is done with numbing drops in a sterile environment similar to an operating room. The participants will return for follow-up visits one month and three months after the injection to check their vision and retina through repeat tests and scans. They are advised to monitor for any signs of complications, such as pain, redness, or changes in vision, and to contact the clinic if these occur.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.20 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Treatment Study
Eligibility
Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.Any sex
Biological sex of participants that are eligible to enroll.Over 18 Years
Range of ages for which participants are eligible to join.Healthy volunteers not allowed
If individuals who are healthy and do not have the condition being studied can participate.Conditions
Pathology
Criteria
Study Plan
Find out more about all the medication administered in this study, their detailed description and what they involve.One single intervention group is designated in this study
This study does not include a placebo group
Treatment Groups
Group I
ExperimentalStudy Objectives
Primary Objectives
Secondary Objectives
Study Centers
These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.This study has 1 location
Ibn Al-Haitham Eye Teaching Hospital
Baghdad, IraqOpen Ibn Al-Haitham Eye Teaching Hospital in Google Maps