Status:

UNKNOWN

Low Dose Atropine for Symptomatic Vitreous Floaters

Lead Sponsor:

Jeanette Du

Conditions:

Vitreous Floaters

Eligibility:

All Genders

19+ years

Phase:

PHASE2

Brief Summary

The objective of this study is to identify a potential pharmacologic option by assessing whether 0.01% atropine may be effective for treating bothersome floaters as measured by scores on a modified NE...

Eligibility Criteria

Inclusion

  • Adult patients within Prism Vision Group with ICD diagnosis of acute posterior vitreous detachment and none of the ocular comorbidities listed as exclusion criteria will be screened as potential study participants.

Exclusion

  • Patients with vitreous hemorrhage, other significant media opacity or vitreoretinal pathology, or history of pars plana vitrectomy will be excluded.

Key Trial Info

Start Date :

January 1 2024

Trial Type :

INTERVENTIONAL

Allocation :

ESTIMATED

End Date :

June 1 2024

Estimated Enrollment :

200 Patients enrolled

Trial Details

Trial ID

NCT06174935

Start Date

January 1 2024

End Date

June 1 2024

Last Update

December 18 2023

Active Locations (1)

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Page 1 of 1 (1 locations)

1

Retina Group of Washington

Reston, Virginia, United States, 20190

Low Dose Atropine for Symptomatic Vitreous Floaters | DecenTrialz