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Effect of Topical Dexmedetomidine on Intraocular Pressure

Phase 4
Completed
Conditions
Intraocular Pressure
Glaucoma
Interventions
Drug: Balanced salt solution
Drug: Dexmedetomidine
Registration Number
NCT03690622
Lead Sponsor
Beirut Eye Specialist Hospital
Brief Summary

Evaluate the short-term safety and efficacy of dexmedetomidine (0.0055%) drops on intraocular pressure (IOP) in healthy eyes.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
49
Inclusion Criteria
  • Patients with healthy eyes and no history of glaucoma
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Exclusion Criteria
  • history of glaucoma, IOP > 24mmHg at baseline, abnormal optic nerve on fundus examination, keratoconus, corneal graft, corneal edema or a history of refractive surgery
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Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
BSSBalanced salt solutionBalanced salt solution
DexmedetomidineDexmedetomidinedexmedetomidine (0.0055%)
Primary Outcome Measures
NameTimeMethod
Intraocular pressure changeat presentation, 30 minutes, 4 hours and 24 hours after instillation

Taken by aplanation tonometry

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Beirut Eye Specialist Hospital

🇱🇧

Beirut, Lebanon

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