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COMPLETED
NCT07774182
NA

Intravitreal Triamcinolone and Biomarkers in Rhegmatogenous Retinal Detachment

Sponsor: Anggun Rama Yudantha

View on ClinicalTrials.gov

Summary

This prospective, randomized, controlled clinical study evaluates the effects of preoperative intravitreal triamcinolone acetonide (TA) on growth factors and inflammatory mediators in patients with rhegmatogenous retinal detachment (RRD) and proliferative vitreoretinopathy (PVR). Participants are assigned to either an intervention group receiving a 2-mg intravitreal injection of TA 5-7 days before vitrectomy or a control group receiving standard surgical treatment. The study evaluates TGF-β2, TGF-β3, MMP-2, and MMP-9 levels in aqueous humor and vitreous, macrophage cell counts and inflammatory activity in vitreous, subretinal fluid optical density assessed by optical coherence tomography, and vessel diameter index assessed by optical coherence tomography angiography after surgery.

Official title: Effect of Intravitreal Triamcinolone Acetonide on TGF-β2, TGF-β3, and Matrix Metalloproteinase Levels in Patients With Rhegmatogenous Retinal Detachment: A Study of Aqueous Humor and Vitreous Biomarkers

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

60

Start Date

2025-05-06

Completion Date

2026-03-18

Last Updated

2026-08-19

Healthy Volunteers

No

Interventions

PROCEDURE

Standard Vitrectomy

Participants underwent standard surgical treatment for rhegmatogenous retinal detachment with proliferative vitreoretinopathy without preoperative intravitreal triamcinolone acetonide.

DRUG

Triamcinolone acetonide (TA)

Triamcinolone acetonide 2 mg was administered by intravitreal injection 5-7 days before vitrectomy.

Locations (1)

Department of Ophthalmology, Faculty of Medicine, Universitas Indonesia - Cipto Mangunkusumo Hospital, Jakarta

Jakarta, DKI Jakarta, Indonesia