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Evaluation of different doses of triamcinolone acetonide in inhibiting anterior uveitis after combined phacoemulsification and trabeculectomy

Evaluation of different doses of triamcinolone acetonide in inhibiting anterior uveitis after combined phacoemulsification and trabeculectomy

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-TRC-12002314
Enrollment
Unknown
Registered
2012-06-29
Start date
2012-01-01
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

Glaucoma

Interventions

Triamcinolone acetonide 0.5:intracameral triamcinolone acetonide 0.5mg in combined phacoemulsification and trabeculectomy
Triamcinolone acetonide 1.0:intracameral triamcinolone acetonide 1.0mg in combined phacoemulsification and trabeculectomy
Triamcinolone acetonide 2.0:intracameral triamcinolone acetonide 2.0mg in combined phacoemulsification and trabeculectomy

Sponsors

Beijing Shijitan Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 76 Years

Inclusion criteria

Inclusion criteria: 1. Over 40 years of age; 2. Patients with visually significant cataract with the best corrected visual acuity less than 0.5; 3. Patients with primary glaucoma with an intraocular pressure of greater than or equal to 22 mmHg despite medical therapy.

Exclusion criteria

Exclusion criteria: 1. Patients with other ocular pathologies such as cornea opacities, uveities, diabetes retinopathy, central retinal vein occlusion, et al.; 2. Secondary glaucoma because of trauma, uveities, neovascularization, et al.; 3. Past medical history of intraocular surgery; 4. Patients taking systemic immunosuppressants or adrenal corticosteroid.

Design outcomes

Primary

MeasureTime frame
Visual Acuity;Intraocular Pressure;Anterior Chamber Inflammation by cells and flar;

Countries

China

Contacts

Public ContactWang Bingsong
wangbingsong@gmail.com+86 15810023101

Outcome results

None listed

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