Clinical Trials Directory

Trials / Terminated

TerminatedNCT06369077

How Much Does Reduced Dosing of Latanoprost and Dorzolamide-timolol Affect Pressure?

Cross-over Comparison of Latanoprost QOD With Dor-tim QAM to Tim-brim-dor-bim(Atoprost) qd or Lat QD With Dor-tim BID

Status
Terminated
Phase
Phase 4
Study type
Interventional
Enrollment
36 (actual)
Sponsor
CT Glaucoma Associates · Academic / Other
Sex
All
Age
25 Years – 90 Years
Healthy volunteers
Accepted

Summary

IOP effect of half-dose latanoprost dorzolamide-timolol will be compared to full dose. Further comparison will be made timolol-brimonidine-dorzolamide-bimatoprost. Dry eye effects of the different treatments will be assessed.

Detailed description

Subjects will have baseline IOP measurements (7-9 am and 3-5 pm) after using using latanoprost every other day and dorzolamide-timolol every morning. They will then randomly be assigned in phase 2 to either: double the frequency to latanoprost daily and dorzolamide-timolol twice daily; or use every morning compounded timolol-brimonidine-dorzolamide-bimatoprost. IOP measurements will be repeated 3 weeks after using the phase 2 medications. For phase 3, subjects will use the treatment to which they were not assigned in phase 2, and IOP measurements will again be repeated 3 weeks later. At each study visit, dry eye signs will be assessed and brief dry eye survey will be administered.

Conditions

Interventions

TypeNameDescription
DRUGdorzolamide/timololCompare half-frequency dosing of latanoprost and dorzolamide/timolol to full dosing. Compare also to timolol/brimonidine/dorzolamide/bimatoprost

Timeline

Start date
2024-04-22
Primary completion
2024-07-30
Completion
2024-07-30
First posted
2024-04-16
Last updated
2024-08-23

Locations

1 site across 1 country: United States

Regulatory

Source: ClinicalTrials.gov record NCT06369077. Inclusion in this directory is not an endorsement.