CompletedPHASE2, PHASE3NCT00853905
Will the Use of Triesence During Glaucoma Surgery Provide Lower Eye Pressure and Improve the Results of the Surgery?
Studying Neovascular glaucoma
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- Wills Eye
- Principal Investigator
- Marlene R Moster, MDWills Eye Institute
- Intervention
- Triesence(drug)
- Enrollment
- 77 target
- Eligibility
- 21 years · All sexes
- Timeline
- 2009 – 2012
Study locations (1)
- Wills Eye Institute, Philadelphia, Pennsylvania, United States
Collaborators
Alcon Research
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
Open NCT00853905 on ClinicalTrials.govOther trials for Neovascular glaucoma
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