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Clinical trial

Intraocular Pressure and Tolerability Study of Preservative Free Bimatoprost 0.03% Unit Dose (BUDPF) or Preservative Free Latanoprost 0.005% Unit Dose (LUDPF) (Monoprost®) in Patients With Ocular Hypertension or Glaucoma: A Randomized, Single Masked, 3 Month Cross-over, Investigator Led, European Multicentre Trial (SPORT)

NCT01975714 is registered in ClinicalTrials.gov with Association for Innovation and Biomedical Research on Light and Image as lead sponsor.

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Registry record

As filed in ClinicalTrials.gov.

Title
Intraocular Pressure and Tolerability Study of Preservative Free Bimatoprost 0.03% Unit Dose (BUDPF) or Preservative Free Latanoprost 0.005% Unit Dose (LUDPF) (Monoprost®) in Patients With Ocular Hypertension or Glaucoma: A Randomized, Single Masked, 3 Month Cross-over, Investigator Led, European Multicentre Trial (SPORT)
Lead sponsor
Association for Innovation and Biomedical Research on Light and Image
Phase
Phase 4
Overall status
Completed
Start date
October 31, 2013
Completion date
February 28, 2015
Enrollment
67 (actual)
Sites
7

Conditions

As the registry lists them; a condition with its own page is linked.