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

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

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07434635
Acronym
APPRAISE
Enrollment
62
Registered
2026-02-25
Start date
2026-02-01
Completion date
2029-02-01
Last updated
2026-02-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Eye Disorders

Keywords

atropine, eye surgery

Brief summary

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

Detailed description

Atropine eyedrops are often used after certain eye surgeries. This study will compare several outcomes following surgery in patients either using or not using this treatment.

Interventions

Subtraction of atropine eyedrops from post-operative treatment regimen

Sponsors

University of California, San Francisco
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Investigator)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* patient undergoing vitrectomy surgery * able to give informed consent

Exclusion criteria

* post-operative eyedrop regimens that include topical non steroidal anti-inflammatory medications * subjects with altered post-operative eyedrop schedule for enhanced inflammation control * documented allergy to atropine

Design outcomes

Primary

MeasureTime frameDescription
Pain score on the Visual Analog Scale (VAS)1 monthWhether atropine use impacts post-operative pain score on the standard Visual Analog Scale (VAS)

Secondary

MeasureTime frameDescription
Anterior chamber inflammation (aqueous cell and flare)1 monthWhether atropine impacts the occurrence of post-operative inflammation, quantified as aqueous cell and flare, using the Standardization of Uveitis Nomenclature (SUN) Criteria
Cystoid macular edema detected by optical coherence tomography1 monthWhether atropine impacts the occurrence of cystoid macular edema after surgery, detected by optical coherence tomography scanning of the retina
Time to visual recovery1 monthWhether atropine impacts the time to visual recovery
Intraocular pressure1 monthWhether atropine impacts intraocular pressure after surgery
Posterior synechiae formation1 monthPresence or absence of posterior synechiae assessed by slit lamp examination at post-operative visits

Countries

United States

Contacts

CONTACTJay Stewart, MD
eyestudy@ucsf.edu415-353-9635
PRINCIPAL_INVESTIGATORJay Stewart, MD

University of California, San Francisco

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 27, 2026