The Ischemic Optic Neuropathy Decompression Trial (IONDT) is a five year study designed to assess the safety and efficacy of optic nerve sheath decompression surgery (ONDS) for non-arteritic ischemic optic neuropathy, diagnosed within one month of onset of visual symptoms. A standardized, common protocol for treatment and data collection will be used by all centers. This multicenter, randomized clinical trial is designed to compare differences in patients randomized to one of two treatment groups as follows: Treatment Group Treatment Sequences No. of Patients 1. Test Treatment Optic Nerve Sheath 150 Decompression 2. Control Treatment Standard Medical Care 150 (no surgery) The primary hypothesis to be addressed by this trial is whether treatment with ONDS is more effective than standard care in (1) restoring or (2) maintaining central visual acuity in patients with NAION? The primary outcome for this trial (change in visual acuity) will be measured using the New York Lighthouse chart. A gain of three or more lines of visual acuity (doubling of the visual angle) will be considered improvement. Secondary outcomes include change in peripheral visual function (using standard Goldman perimetry) and incidence ophthalmic and systemic complications. Patients will be recruited over a two year period and followed for a minimum of one year. Study Centers will include a Chairman's Center, 26 Clinical Centers, and centralized facilities, including a Coordinating Center, a Reading Center, and a Project Office at the National Eye Institute.

Agency
National Institute of Health (NIH)
Institute
National Eye Institute (NEI)
Type
Cooperative Clinical Research--Cooperative Agreements (U10)
Project #
3U10EY009556-03S1
Application #
2163167
Study Section
Vision Research and Training Committee (VSN)
Project Start
1994-06-01
Project End
1996-11-30
Budget Start
1994-06-01
Budget End
1996-11-30
Support Year
3
Fiscal Year
1995
Total Cost
Indirect Cost
Name
Saint Louis University
Department
Ophthalmology
Type
Schools of Medicine
DUNS #
City
Saint Louis
State
MO
Country
United States
Zip Code
63103
Scherer, Roberta W; Feldon, Steven E; Levin, Lori et al. (2008) Visual fields at follow-up in the Ischemic Optic Neuropathy Decompression Trial: evaluation of change in pattern defect and severity over time. Ophthalmology 115:1809-17
Newman, Nancy J (2007) The ischemic optic neuropathy decompression trial. Arch Ophthalmol 125:1568-70
Feldon, Steven E; Levin, Lori; Scherer, Roberta W et al. (2006) Development and validation of a computerized expert system for evaluation of automated visual fields from the Ischemic Optic Neuropathy Decompression Trial. BMC Ophthalmol 6:34
Scherer, Roberta; Zhu, Qi; Langenberg, Patricia et al. (2003) Comparison of information obtained by operative note abstraction with that recorded on a standardized data collection form. Surgery 133:324-30
Feldon, Steven E; Scherer, Roberta W; Hooper, Frank J et al. (2003) Surgical quality assurance in the Ischemic Optic Neuropathy Decompression Trial (IONDT). Control Clin Trials 24:294-305
Newman, Nancy J; Scherer, Roberta; Langenberg, Patricia et al. (2002) The fellow eye in NAION: report from the ischemic optic neuropathy decompression trial follow-up study. Am J Ophthalmol 134:317-28
(2000) Ischemic Optic Neuropathy Decompression Trial: twenty-four-month update. Arch Ophthalmol 118:793-8
(1998) The ischemic optic neuropathy decompression trial (IONDT): design and methods. Control Clin Trials 19:276-96
Crawley, B; Scherer, R; Langenberg, P et al. (1997) Participation in the Ischemic Optic Neuropathy Decompression Trial: sex, race, and age. Ophthalmic Epidemiol 4:157-73
(1996) Characteristics of patients with nonarteritic anterior ischemic optic neuropathy eligible for the Ischemic Optic Neuropathy Decompression Trial. Arch Ophthalmol 114:1366-74

Showing the most recent 10 out of 11 publications