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Intravitreal triamcinolone acetonide combined withccataract surgery for diabetic macular edema

Intravitreal triamcinolone acetonide combined withccataract surgery for diabetic macular edema - IVTA with cataract for DME

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
JPRN
Registry ID
JPRN-UMIN000029818
Enrollment
30
Registered
2017-11-04
Start date
2015-11-25
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

diabetic macular edema

Interventions

None listed

Sponsors

Department of Ophthalmology, Mie University Graduate School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: All of the patients had received IVTA combined with phacoemulsification and aspiration cataract surgery and intraocular lens implantation between December 2014 and December 2016. The inclusion criteria were patients who were resistant to previous treatments such as retinal photocoagulation, intravitreal injections of anti-VEGF agents, or sub-tenon triamcinolone acetonide injections(STTA), had a medical history of systemic diseases such as myocardial infarction, cerebral infarction, or cerebral hemorrhage, and had financial difficulty in paying for the anti-VEGF treatments. The CRT of all the patients was over 300 um as determined by fluorescein angiography(FAG)and optical coherence tomography(OCT). A recurrence was defined as an increase in the CRT by 20% compared to the minimum CRT value during the observation period.

Exclusion criteria

Exclusion criteria: Patients were excluded if they had the macular traction syndrome, active proliferative diabetic retinopathy, uveitis, poorly controlled ocular hypertension, glaucoma, had intraocular surgery within the past 6 months, and history of anti-VEGF treatment or STTA, or had macular photocoagulation within the past 3 months before the beginning of the treatment. Patients who had adverse reactions to steroids were also excluded.

Design outcomes

Primary

MeasureTime frame
Visual acuity after treatment

Countries

Japan

Contacts

Public ContactMasahiko Sugimoto

Mie University Graduate School of Medicine Department of Ophthalmology

sugmochi@aqua.ocn.ne.jp059-232-1111

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026