Evaluation of Vitrase as an Adjuvant to Increase Absorption and Dispersion of Other Injected Anesthetics
Completed · Phase 4
Conditions studied: Pain
In brief
The purpose of this study is to evaluate Vitrase as an adjuvant to increase absorption and dispersion of other injected anesthetics
Key facts
- Study ID
- NCT00198549
- Run by
- Bausch & Lomb Incorporated
- People needed
- 40
- Starts
- 2004-09-01
- Expected to finish
- 2005-03-01
- Last updated by the study team
- 2013-03-19
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Scheduled for an ophthalmic surgical procedure
You may not qualify if…
- Known allergy to bee venom
Where it is running
- Cincinnati Eye Institute — Cincinnati, Ohio, United States
Full record on ClinicalTrials.gov
Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.