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NCT06174935

Low Dose Atropine for Symptomatic Vitreous Floaters

Status unknown Phase 2 Last updated 18 December 2023
What this trial tests

Phase 2 trial testing 0.01% atropine ophthalmic drop in Vitreous Floaters in 200 participants. Status unknown.

Timeline
1 January 2024
Primary endpoint
1 June 2024
1 June 2024

Quick facts

Lead sponsorJeanette Du
PhasePhase 2
StatusStatus unknown
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposetreatment
Enrollment200
Start date1 January 2024
Primary completion1 June 2024
Estimated completion1 June 2024
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

Jeanette Du — full company profile →

Who can join

19 and older, any sex, with Vitreous Floaters. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

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 NEI VFQ-25.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Vitreous Floaters

Currently open trials in the same condition.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06174935.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing