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Search / Trial NCT06213649

Parasitic Ulcer Treatment Trial

Launched by JEREMY KEENAN, MD, MPH · Jan 9, 2024

Trial Information

Current as of August 19, 2025

Recruiting

Keywords

Corneal Ulcer Steroids

ClinConnect Summary

The Parasitic Ulcer Treatment Trial (PUTT) is a research study looking at how adding a certain type of medication called corticosteroids to the treatment for acanthamoeba keratitis (AK) can help improve vision. Acanthamoeba keratitis is an eye infection caused by a type of parasite that can lead to inflammation and discomfort. To participate in this trial, patients need to have signs of ocular inflammation after four weeks of standard treatment for AK. Eligible participants must be 21 years or older and show evidence of the infection through various medical tests.

If you join the trial, you'll be randomly placed into one of two groups: one group will receive the corticosteroid treatment, while the other group will receive a placebo, which looks like the actual medication but has no active ingredients. Throughout the trial, participants will be closely monitored to see how well their vision improves. It's important to note that some people may not qualify, such as those with certain other eye conditions or allergies to steroids. This study is currently recruiting participants, and you can expect a supportive environment with regular check-ins about your progress.

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • AK on at least one of the following: culture, smear, PCR, shotgun sequencing, biopsy, or confocal microscopy
  • Ocular inflammation after 1 month of anti-amoebic treatment, defined as conjunctival, corneal, episcleral, or anterior chamber inflammation
  • Exclusion Criteria:
  • Evidence or history of interstitial keratitis
  • Known herpetic keratitis, as determined from history, exam, or microbiological testing
  • Known fungal keratitis, as demonstrated from corneal scrapings
  • Corneal perforation or impending corneal perforation
  • Prior therapeutic keratoplasty for acanthamoeba keratitis
  • Unwillingness or inability to follow-up
  • No light perception in the affected eye
  • Known hypertensive response to steroids
  • Corticosteroid allergy
  • Concurrent treatment with systemic corticosteroids
  • Concurrent granulomatous amoebic encephalitis

About Jeremy Keenan, Md, Mph

Dr. Jeremy Keenan, MD, MPH, is a distinguished clinical trial sponsor known for his commitment to advancing medical research and improving patient outcomes. With a robust background in medicine and public health, Dr. Keenan leads innovative clinical trials that focus on addressing critical health challenges. His expertise encompasses a wide range of therapeutic areas, and he is dedicated to fostering collaboration among multidisciplinary teams to ensure the highest standards of research integrity and ethical practices. Through his leadership, Dr. Keenan aims to translate scientific findings into tangible benefits for patients and the broader healthcare community.

Locations

Philadelphia, Pennsylvania, United States

New York, New York, United States

Los Angeles, California, United States

Baltimore, Maryland, United States

San Francisco, California, United States

Iowa City, Iowa, United States

Miami, Florida, United States

Portland, Oregon, United States

Chicago, Illinois, United States

London, , United Kingdom

Coimbatore, Tamil Nadu, India

Madurai, Tamil Nadu, India

São Paulo, , Brazil

Madurai, Tamil Nadu, India

Gainesville, Florida, United States

Patients applied

0 patients applied

Trial Officials

Jeremy Keenan, MD, MPH

Principal Investigator

Proctor Foundation, UCSF

Gerami Seitzman, MD

Principal Investigator

Proctor Foundation, UCSF

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported