Skip to content

IOP Reduction After Anecortave Acetate Injection in Glaucoma Patients

Anterior Juxtascleral Depot of Anecortave Acetate: Intraocular Pressure Reduction in Glaucoma Patients

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00533962
Enrollment
30
Registered
2007-09-24
Start date
2007-08-31
Completion date
Unknown
Last updated
2007-09-24

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

Conditions

Glaucoma, Intraocular Pressure

Keywords

Glaucoma, Anecortave Acetate, Intraocular pressure, Advanced glaucoma cases with uncontrolled IOP

Brief summary

Introduction: Ocular administration of glucocorticoids is a common and effective treatment for several ocular diseases. However it is often complicated with the elevation of intraocular pressure (IOP). Anecortave acetate (AA) is an analog of cortisol acetate and lacks the typical anti-inflammatory and immunosuppressive properties of glucocorticoids. The effect of its anterior juxtascleral depot (AJD) injection has been evaluated in cases of glaucoma caused by intravitreal triamcinolone acetonide, presenting impressive results. The purpose of this study is to evaluate the efficacy and safety of the AA injection as a possible antiglaucoma treatment alternative. Methods: A prospective clinical study will be carried out including 30 glaucoma patients (30 eyes). After inclusion each patient will receive a single AJD injection of 30 mg of AA in the selected eye. Main outcome measure include: intraocular pressure at 1st day, 7th day, 1st, 2nd and 3rd months.

Interventions

DRUGAnterior Juxtascleral Depot of Anecortave Acetate

Sponsors

Alcon Research
CollaboratorINDUSTRY
Federal University of São Paulo
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* Advanced glaucoma cases with surgery or cyclophotocoagulation indication (IOP over 25 mmHg) * Patients should be under maximum tolerated medication * Low best corrected visual acuity (worse than 20/100)

Exclusion criteria

* Under 18 or over 80

Design outcomes

Primary

MeasureTime frame
Intraocular pressureProcedure

Secondary

MeasureTime frame
Visual Acuity; side effects (biomicroscopy exam)Post treatment

Countries

Brazil

Outcome results

None listed

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