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Clinical Trials/NCT01801774
NCT01801774
Unknown
Phase 4

Quantitative Comparison of the Efficacy of Subtenon 20-mg Triamcinolone Injection With 0.1% Dexamethasone Eye Drop in Controlling Intraocular Inflammation After Phacoemulsification

Mahidol University1 site in 1 country140 target enrollmentMay 2012

Overview

Phase
Phase 4
Intervention
Placebo
Conditions
Inflammation
Sponsor
Mahidol University
Enrollment
140
Locations
1
Primary Endpoint
Anterior chamber reaction
Last Updated
11 years ago

Overview

Brief Summary

Phacoemulsification is a quick method with less complication for cataract surgery. Due to the use of ultrasonic energy, it produced more post-operative inflammation than other methods. Many routes of steroid had been used to control post-operative inflammation. The investigators here compare the efficacy of single depot steroid subtenon injection (20-mg triamcinolone) with four-time-a-day steroid eye drop (0.1% dexamethasone) in controlling inflammation after uneventful phacoemulsification.

Detailed Description

Cataract is one of the most common causes of blindness in the world. Surgical removal of lens is the only treatment for cataract, which now shifts from extracapsular cataract extraction to phacoemulsification. Although phacoemulsification provides faster operating time and gives better optical result and rapid recovery to the patient, it causes more inflammation post-operatively compare with extracapsular cataract extraction. Corticosteroids eye drops are mainly use to control intraocular inflammation after the surgery. Other routes of corticosteroids have been introduced to increase the intraocular level and to increase the patient's compliance. Subtenon triamcinolone injection is easy and safe. Antiinflammatory effect of single subtenon triamcinolone injection lasts about 4-6 weeks. This method has been used in combination with corticosteroid eye drop to control the inflammation after cataract surgery in uveitic patients. It shows potency in controlling of intraocular inflammation with lower rate of increasing the intraocular pressure. The investigators here quantitatively compare the efficacy of subtenon 20-mg triamcinolone injection with 0.1% dexamethasone eye drop in controlling intraocular inflammation after uneventful phacoemulsification.

Registry
clinicaltrials.gov
Start Date
May 2012
End Date
July 2015
Last Updated
11 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Age older than 18 years old
  • Uncomplicated cataract patient scheduled for phacoemulsification and posterior chamber intraocular lens implantation
  • No History of prior intraocular procedures or any eye diseases such as uveitis, glaucoma, diabetic retinopathy
  • No History of systemic autoimmune diseases
  • No History of allergy to corticosteroids or to any component of the study medications
  • No History of using corticosteroids, non-steroidal anti-inflammatory drugs (NSAIDs), or immunomodulating agents within 3 months prior to surgery

Exclusion Criteria

  • Complications occurred during cataract surgery such as ruptured posterior capsule, vitreous loss, or dropped nucleus
  • Pregnant and lactating women

Arms & Interventions

Dexamethasone

Dexamethasone 0.1%/Tobramycin 0.3% eye drop 4 times per day for 28 days

Intervention: Placebo

Triamcinolone

Subtenon 20-mg Triamcinolone injection

Intervention: Subtenon 20-mg triamcinolone injection

Outcomes

Primary Outcomes

Anterior chamber reaction

Time Frame: postoperative day 28

proportion of anterior chamber reaction grade 0 measured by anterior chamber inflammation score at postoperative day 28+/-5

Secondary Outcomes

  • rate of increased intraocular pressure over 21 mmHg(preoperative, postoperative day 1,7,14,28,90)
  • Changes of anterior chamber reaction over time(preoperative, postoperative day1, 7, 14, 28, 90)

Study Sites (1)

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