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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT01511094
Other study ID # Gonio-32
Secondary ID
Status Active, not recruiting
Phase Phase 2/Phase 3
First received October 14, 2011
Last updated January 17, 2012
Start date June 2009
Est. completion date January 2012

Study information

Verified date January 2012
Source Federal University of Minas Gerais
Contact n/a
Is FDA regulated No
Health authority Brazil: National Committee of Ethics in Research
Study type Interventional

Clinical Trial Summary

The study has the purpose to evaluate the effectiveness and safety of the goniocurettage as a first choice of surgical treatment for primary open-angle glaucoma (POAG) in patients with good vision.


Description:

A prospective study in 33 eyes (32 patients) with uncontrolled open angle glaucoma under clinical treatment. The trabecular tissue was scraped away from the angle (goniocurettage) in about 100 degrees by means of an instrument similar to a microchalazion curette. The goniocurettage was done under direct visualization of the angle through a gonioscopy lens (Swan-Jacob) and a surgical microscope. Using the 17.0 SPSS software the investigators compared the intraocular pressure, the numbers of antiglaucomatous medications, the best correct visual acuity, the development of cataract, the central corneal thickness,the impact on the visual field, the impact on the optic nerve head and the central corneal endothelial cell density before and after the goniocurettage, and the intra and post operative complications.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 32
Est. completion date January 2012
Est. primary completion date May 2010
Accepts healthy volunteers No
Gender Both
Age group 40 Years and older
Eligibility Inclusion Criteria:

- Disc and/or visual field findings consistent with Primary Open Angle Glaucoma

- Uncontrolled intraocular pressure (=21 mm Hg) or progressive glaucomatous neuropathy despite maximum tolerated medical therapy

- 40 years old or over

- Visual acuity higher than 0.2

- Open angles (greater or equal to Shaffer grade II)

Exclusion Criteria:

- Previous ocular surgery

- History of glaucoma laser treatment

- History of ocular trauma

- Cyclodestructive procedures

- Corneal edema or opacities

- Endothelial decompensation

- History of uveitis

- Secondary glaucoma

- neovascularization of the iris or angle

- Congenital anterior segment abnormalities

- Anatomically confusing angles without clear definition of the scleral spur or meshwork and inability to maintain follow-up

Study Design

Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Procedure:
Goniocurettage
Ab interno surgery consisting on scraped away the trabecular tissue from the angle (goniocurettage) removing segments of pathologically altered trabecular meshwork from the scleral sulcus

Locations

Country Name City State
Brazil Federal University of Minas Gerais Belo Horizonte Minas Gerais

Sponsors (1)

Lead Sponsor Collaborator
Federal University of Minas Gerais

Country where clinical trial is conducted

Brazil, 

References & Publications (5)

Jacobi PC, Dietlein TS, Krieglstein GK. Goniocurettage for removing trabecular meshwork: clinical results of a new surgical technique in advanced chronic open-angle glaucoma. Am J Ophthalmol. 1999 May;127(5):505-10. — View Citation

Jacobi PC, Dietlein TS, Krieglstein GK. Microendoscopic trabecular surgery in glaucoma management. Ophthalmology. 1999 Mar;106(3):538-44. — View Citation

Jacobi PC, Dietlein TS, Krieglstein GK. Technique of goniocurettage: a potential treatment for advanced chronic open angle glaucoma. Br J Ophthalmol. 1997 Apr;81(4):302-7. — View Citation

Johnson DH, Johnson M. How does nonpenetrating glaucoma surgery work? Aqueous outflow resistance and glaucoma surgery. J Glaucoma. 2001 Feb;10(1):55-67. Review. — View Citation

Minckler D, Baerveldt G, Ramirez MA, Mosaed S, Wilson R, Shaarawy T, Zack B, Dustin L, Francis B. Clinical results with the Trabectome, a novel surgical device for treatment of open-angle glaucoma. Trans Am Ophthalmol Soc. 2006;104:40-50. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Intra Ocular Pressure The mean of at least three measures at 8:00 am two weeks before surgery. After intervention, the Intra Ocular Pressure was measured on the day after, one week after, two weeks after and every month at the same time until the end of the study (an expected average of 20 months). Change from Baseline in Intra Ocular Pressure at 20 months Yes
Secondary Central Corneal Thickness Two weeks before, six months after and one year after intervention Yes
Secondary Central corneal endothelial cell density Two weeks before, six months after intervention and one year after intervention Yes
Secondary Best correct visual acuity Two weeks before, six months after and one year after intervention Yes
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