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Use of Intravitreal Triamcinolone and Retrobulbar Chlorpromazine as Alternatives to the Management of Painful Blind Eye

Use of Intravitreal Triamcinolone and Retrobulbar Chlorpromazine as Alternatives to the Management of Painful Blind Eye

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01404364
Enrollment
36
Registered
2011-07-28
Start date
2010-01-31
Completion date
2010-12-31
Last updated
2011-07-28

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

Conditions

Blind Painful Eye, Refractory Glaucoma, Control of Pain Through Drug Injection

Keywords

Triamcinolone, Chlorpromazine, Refractory glaucoma, Blind painful eye

Brief summary

The purpose of this study is to evaluate the efficacy of intravitreal triamcinolone and retrobulbar chlorpromazine as alternatives in the management of ocular pain in blind eyes.

Detailed description

The management of chronic eye pain is a constant challenge to ophthalmology. Treatment varies with the intensity of pain, and topical eye drops and contact lens therapy are effective in many patients. In refractory cases, and without vision, surgical removal of the eye through enucleation is considered classical therapy. As less invasive alternatives we have cyclodestruction and neurolytic drug injection in order to promote analgesia for a prolonged period. The purpose of this study is to evaluate the efficacy of intravitreal triamcinolone and retrobulbar chlorpromazine as alternatives in the management of This is a prospective study of patients with blind painful eyes not responsive to topical treatment and with no indication for evisceration seen at the Department of Ophthalmology, Hospital Governador Celso Ramos (HGCR) in 2010.

Interventions

DRUGTriamcinolone

0,3mL intravitreal injection of Triamcinolone, single dose

2,5mL Chlorpromazine retrobulbar injection, single dose

Sponsors

Hospital Governador Celso Ramos
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
15 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* patients treated in the period at HGCR who wanted to be part of the protocol by signing the consent form

Exclusion criteria

* patients whose follow-up period was less than three months

Design outcomes

Primary

MeasureTime frameDescription
Changes in Pain intensity0, 1 month, 3 months, 6 months after procedurePain was measured asking the patient to graduate it in a scale from 0 to 10, 0 being no pain, 10 being the worst pain patient has experienced in life

Secondary

MeasureTime frameDescription
Changes in Use of eyedrops before and after drug injection0, 1 month, 3 months, 6 monthsPatient use of eyedrops before and after the procedure (yes or no)
Changes in Intraocular pressure (IOP)0, 1 months, 3 months, 6 monthsIOP was measured at all times of patient evaluation

Countries

Brazil

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026