Actively Recruiting

Phase 4
Age: 18Years +
All Genders
NCT07434635

APPRAISE: Assessment of Pain and Posterior Synechiae Reduction With Atropine, an Investigation of Post-Surgical Eyes

Led by University of California, San Francisco · Updated on 2026-02-25

62

Participants Needed

1

Research Sites

156 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The study will evaluate whether atropine eyedrops are beneficial when used after certain eye surgeries.

CONDITIONS

Official Title

APPRAISE: Assessment of Pain and Posterior Synechiae Reduction With Atropine, an Investigation of Post-Surgical Eyes

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patient undergoing vitrectomy surgery
  • Able to give informed consent
Not Eligible

You will not qualify if you...

  • Use of post-operative eyedrop regimens that include topical non steroidal anti-inflammatory medications
  • Altered post-operative eyedrop schedule for enhanced inflammation control
  • Documented allergy to atropine

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

University of California, San Francisco

San Francisco, California, United States, 94143

Actively Recruiting

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Research Team

J

Jay Stewart, MD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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