Actively Recruiting

Phase 3
Age: 8Years +
All Genders
NCT06213649

Parasitic Ulcer Treatment Trial

Led by Jeremy Keenan, MD, MPH · Updated on 2026-05-01

232

Participants Needed

17

Research Sites

260 weeks

Total Duration

On this page

Sponsors

J

Jeremy Keenan, MD, MPH

Lead Sponsor

J

Johns Hopkins University

Collaborating Sponsor

AI-Summary

What this Trial Is About

The Parasitic Ulcer Treatment Trial (PUTT) is a multi-center, parallel-group, randomized clinical trial. The purpose of this study is to determine whether including topical corticosteroids in a regimen for acanthamoeba keratitis (AK) will improve vision. Patients presenting to all enrollment centers with evidence of acanthamoeba keratitis will be eligible for the trial if there is evidence of ocular inflammation after 4 weeks of anti-amoebic therapy. Those who agree to participate will be randomized to one of two treatment groups: * Group 1: Topical corticosteroid * Group 2: Topical placebo

CONDITIONS

Official Title

Parasitic Ulcer Treatment Trial

Who Can Participate

Age: 8Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Acanthamoeba keratitis confirmed by culture, smear, PCR, shotgun sequencing, biopsy, or confocal microscopy
  • Evidence of ocular inflammation after at least 1 month of anti-amoebic treatment, including inflammation of the conjunctiva, cornea, episclera, or anterior chamber
  • Age 8 years or older
Not Eligible

You will not qualify if you...

  • History or evidence of interstitial keratitis
  • Known herpetic keratitis based on history, exam, or microbiological testing
  • Known fungal keratitis confirmed by corneal scrapings
  • Corneal perforation or risk of imminent corneal perforation
  • Previous therapeutic keratoplasty for acanthamoeba keratitis
  • Unwillingness or inability to participate in follow-up visits
  • No light perception in the affected eye
  • Known hypertensive response to steroids
  • Allergy to corticosteroids
  • Current treatment with systemic corticosteroids
  • Concurrent granulomatous amoebic encephalitis

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 17 locations

1

University of California, San Francisco

San Francisco, California, United States, 94158

Actively Recruiting

2

University of Colorado Anschutz

Aurora, Colorado, United States, 80045

Actively Recruiting

3

University of Florida

Gainesville, Florida, United States, 32605

Actively Recruiting

4

University of Miami

Miami, Florida, United States, 33136

Actively Recruiting

5

University of Illinois, Chicago

Chicago, Illinois, United States, 60612

Actively Recruiting

6

University of Iowa

Iowa City, Iowa, United States, 52242

Actively Recruiting

7

Johns Hopkins University

Baltimore, Maryland, United States, 21287

Actively Recruiting

8

Columbia University

New York, New York, United States, 10032

Actively Recruiting

9

Oregon Health and Science University

Portland, Oregon, United States, 97239

Actively Recruiting

10

University of Pennsylvania

Philadelphia, Pennsylvania, United States, 19104

Actively Recruiting

11

University of Pittsburgh Medical Center

Pittsburgh, Pennsylvania, United States, 15219

Actively Recruiting

12

Baylor College of Medicine

Houston, Texas, United States, 77030

Actively Recruiting

13

University of Washington

Seattle, Washington, United States, 98104

Actively Recruiting

14

Federal University of São Paulo

São Paulo, Brazil

Actively Recruiting

15

Aravind Eye Hospital

Coimbatore, Tamil Nadu, India

Actively Recruiting

16

Aravind Eye Hospital

Madurai, Tamil Nadu, India

Actively Recruiting

17

Moorfields Eye Hospital

London, United Kingdom

Actively Recruiting

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Research Team

J

Jeremy Keenan, MD, MPH

CONTACT

K

Krisi Aromin

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

QUADRUPLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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