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The Role of Steroids Following Selective Laser Trabeculoplasty

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT00406042
First Posted: December 4, 2006
Last Update Posted: March 29, 2007
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by:
West Virginia University
  Purpose
To evaluate whether or not using topical steroids after selective laser trabeculoplasty affects intraocular pressure outcomes.

Condition Intervention
Glaucoma Drug: prednisolone acetate 1%

Study Type: Interventional
Study Design: Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Single
Primary Purpose: Treatment
Official Title: The Role of Topical Prednisolone Acetate Following Selective Laser Trabeculoplasty

Resource links provided by NLM:


Further study details as provided by West Virginia University:

Primary Outcome Measures:
  • Intraocular pressure reduction

Secondary Outcome Measures:
  • Anterior chamber inflammation

Estimated Enrollment: 25
Study Start Date: September 2005
Study Completion Date: June 2006
Detailed Description:
Subjects undergoing bilateral SLT will be randomly assigned to use prednisolone acetate 1% in one eye four times daily with no treatment in the fellow eye, for one week following SLT. Examinations will occur at baseline, and one week, one month and three months after SLT. IOP and anterior chamber inflammation will be noted at each visit.
  Eligibility

Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years and older   (Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • glaucoma or ocular hypertension
  • need for bilateral SLT

Exclusion Criteria:

  • eye disease precluding accurate IOP measurement
  • contraindication to topical prednisolone acetate
  Contacts and Locations
Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00406042


Locations
United States, West Virginia
West Virginia University Eye Institute
Morgantown, West Virginia, United States, 26505
Sponsors and Collaborators
West Virginia University
Investigators
Principal Investigator: Tony Realini, MD West Virginia University Eye Institute
  More Information

Publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
ClinicalTrials.gov Identifier: NCT00406042     History of Changes
Other Study ID Numbers: 16678
First Submitted: November 29, 2006
First Posted: December 4, 2006
Last Update Posted: March 29, 2007
Last Verified: March 2007

Keywords provided by West Virginia University:
glaucoma
trabeculoplasty
steroids

Additional relevant MeSH terms:
Glaucoma
Ocular Hypertension
Eye Diseases
Prednisolone acetate
Methylprednisolone acetate
Prednisolone
Methylprednisolone
Methylprednisolone Hemisuccinate
Prednisolone hemisuccinate
Prednisolone phosphate
Anti-Inflammatory Agents
Glucocorticoids
Hormones
Hormones, Hormone Substitutes, and Hormone Antagonists
Physiological Effects of Drugs
Antineoplastic Agents, Hormonal
Antineoplastic Agents
Antiemetics
Autonomic Agents
Peripheral Nervous System Agents
Gastrointestinal Agents
Neuroprotective Agents
Protective Agents