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Anti-inflammatory Effect of Triamcinolone Acetonide in Acute Primary Angle-Closure Patients Receiving Phacoemulsification and Intraocular Lens Implantation

Anti-inflammatory Effect of Triamcinolone Acetonide in Acute Primary Angle-Closure Patients Receiving Phacoemulsification and Intraocular Lens Implantation

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1900021009
Enrollment
Unknown
Registered
2019-01-24
Start date
2016-06-01
Completion date
Unknown
Last updated
2019-01-28

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

Conditions

Cataracts, glaucoma

Interventions

Group 2:subconjunctival injectiointracameral injection of triamcinolone acetonide (0.5mg)
Group 1:subconjunctival injection of dexamethasone (3mg)
Group 3:subconjunctival injectiointracameral injection of triamcinolone acetonide (1.0mg)
Group 4:subconjunctival injectiointracameral injection of triamcinolone acetonide (1.5mg)

Sponsors

Chinese PLA General Hospital
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
58 Years to 72 Years

Inclusion criteria

Inclusion criteria: Patients were diagnosed for APAC if they presented at least two typical symptoms (ocular or periocular pain, nausea or vomiting, blurry or halo vision); and showed acute increase in IOP to level > 40 mmHg (by Goldmann applanation tonometry) in conjunction with at least 3 of the signs (conjunctival injection, corneal epithelial edema, mid-dilated unreactive pupil, shall anterior chamber, glaucomflecken, and iris atrophy). No evidence of secondary glaucoma such as neovascular glaucoma, and uveitic glaucoma[18]. Recruited patients showed APAC that could be managed using anti-glaucomatous medications or paracentesis, and demonstrated IOP drop to level < 25 mmHg within 24 hours after treatment was administered.

Exclusion criteria

Exclusion criteria: Patients with hypermature cataract, secondary glaucoma, ocular trauma, history of infectious and noninfectious uveitis, and previous ocular surgeries were excluded. Patients with autoimmune diseases who take glucocorticoids or immunosuppressants were excluded. Patients showing posterior capsular rupture, iris bleeding and injury during surgery, and those could not be regularly followed up were also excluded.

Design outcomes

Primary

MeasureTime frame
Anterior chamber flare;Anterior chamber cells;

Secondary

MeasureTime frame
Visual acuity;introccular pressure;

Countries

China

Contacts

Public ContactLiexi Jia

Chinese PLA general Hospital

jialiexi@163.com+86 13901074337

Outcome results

None listed

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