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A study to compare post-operative inflammation between subconjunctival triamcinolone acetate versus prednisolone drops group after cataract surgery

A Comparative study of subconjunctival triamcinolone acetate versus topical steroid for control of inflammation after phacoemulsification surgery. - NONE

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/02/049635
Enrollment
100
Registered
2023-02-10
Start date
Unknown
Completion date
Unknown
Last updated
2023-03-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: H25- Age-related cataract

Interventions

Intervention1: SUBCONJUNCTIVAL TRIAMCINOLONE ACETATE: Subconjunctival triamcinolone acetate (20 mg in 0.5 ml) will be given to group A. 0.5 ml of fluid from 40mg/ml vial of triamcinolone acetate (comm

Sponsors

GGSMCH Faridkot
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients with age related cataract who can be taken up for uncomplicated phacoemulsification surgery (Nuclear opalescence grade 2-5 , cortical grade 2-5, posterior subcapsular grade 2-5 according LOCS III classification

Exclusion criteria

Exclusion criteria: 1 Known allergy to any of the contents of the pharmaceuticals used in the study 2 Posterior polar cataract 3 Uveitis 4 Glaucoma 5 Cystoid macular edema ( clinically significant ) 6 Retinal abnormality causing cystoid macular edema eg diabetes, vein occlusion, subretinal neovascular membrane. 7 Exclusion after enrollment: significant complications to surgery such as posterior capsule rupture, vitreous loss and dislocated lens or cortical material. These surgical complications may cause excessive inflammation and these patients would be excluded from the study.

Design outcomes

Primary

MeasureTime frame
Control of inflammation measured by: 1. Anterior chamber inflammation 2. central sub foveal thickness - OCTTimepoint: 6 weeks for each patient; 1.5-2 year for whole study

Secondary

MeasureTime frame
To record the post operative adverse effects including intraocular pressure (IOP), subconjunctival hemorrhage of subconjunctival triamcinolone acetate in comparison to topical steroid eye dropsTimepoint: 6 weeks for each patient; 1.5-2 year for whole study

Countries

India

Contacts

Public ContactHarshita moond

GGSMCH faridkot

neha.knew@gmail.com7009909238

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026