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The Results of Ahmed Valve Operations

A Comparison Between Superior and Inferior Ahmed Glaucoma Valve Implantation: Surgical Success and Complications

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT00193960
Enrollment
80
Registered
2005-09-19
Start date
1997-01-31
Completion date
2005-06-30
Last updated
2005-12-01

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

Conditions

Glaucoma

Keywords

Seton surgery, glaucoma, Ahmed valve, intraocular pressure

Brief summary

Glaucoma drainage devices are usually placed in the superior quadrants. The superotemporal quadrant is usually the site of choice. However, when the upper fornix is scarred and especially when conjunctiva is two fibrotic to enable adequate coverage of tube with a scleral or other patch graft, some surgeons place the tube in one of inferior quadrants.

Detailed description

Glaucoma drainage devices are usually placed in the superior quadrants. The superotemporal quadrant is usually the site of choice. However, when the upper fornix is scarred and especially when conjunctiva is two fibrotic to enable adequate coverage of tube with a scleral or other patch graft, some surgeons place the tube in one of inferior quadrants. In the present study we will compare the outcome and complicatons of both the superior and the inferior approach for inserting Ahmed Valve implants.

Interventions

PROCEDURE1) Intraocular pressure 2) visual acuity

Sponsors

University Health Network, Toronto
Lead SponsorOTHER

Study design

Observational model
DEFINED_POPULATION
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
20 Years to 85 Years
Healthy volunteers
No

Inclusion criteria

1. Patients at the ages of 20-85 on the date of the surgery 2. The indication for the surgery was: uncontrolled glaucoma with maximally tolerated medical therapy who did not or were not expected to respond to other surgical procedures than seton surgery. 3. Visual acuity of, at least, 20/800 before the operation. 4. Regular post operative follow ups, for at least 1 year. 5. Patients after corneal transplantation for whom the indication of valve implantation was uncontrolled glaucoma.

Exclusion criteria

1. A previous seton surgery in the operated eye 2. Uveitic glaucoma patients or history of uveitis in the operated or in the fellow eye. 3. Any inflammatory or ocular surface disease that could affect the healing of the conjunctiva after the surgery ( e.g: OCP) 4. Strabismus or complains of diplopia prior to the seton surgery. 5. Past history of retinal detachment surgery with scleral buckle in the operated eye 6. Past history of endophthalmitis in the operated eye.

Countries

Canada

Contacts

Primary ContactRony Rachmiel, M.D.
rachmiel_r@hotmail.com416-603-5317

Outcome results

None listed

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