Parasitic Ulcer Treatment Trial Pilot
Primary Purpose
Acanthamoeba Keratitis
Status
Active
Phase
Phase 2
Locations
India
Study Type
Interventional
Intervention
Chlorhexidine
Povidone-Iodine
Prednisolone Sodium Phosphate
Hydroxypropyl Methylcellulose
Prednisolone Sodium Phosphate
Hydroxypropyl Methylcellulose
Sponsored by
About this trial
This is an interventional treatment trial for Acanthamoeba Keratitis
Eligibility Criteria
Trial 1 Inclusion Criteria:
- Smear or culture positive for acanthamoeba
- Age 13 years or greater
Trial 1 Exclusion Criteria:
- Interstitial or viral keratitis on history or examination
- Corneal perforation
- Therapeutic keratoplasty for acanthamoeba keratitis
- Unwillingness or inability to follow-up (e.g., living too far from hospital)
Trial 2 Inclusion Criteria
- Smear or culture positive for acanthamoeba, with 4 weeks of anti-amoebic treatment
- Age 13 years or greater
- Willing to participate in study
Trial 2 Exclusion Criteria
- Interstitial or viral keratitis on history or examination
- Fungus identified on culture and smear after 2 weeks of anti-amoebic treatment
- Corneal perforation
- Therapeutic keratoplasty for acanthamoeba keratitis
- Unwillingness or inability to follow-up (e.g., living too far from hospital)
Sites / Locations
- Aravind Eye Hospital
- Aravind Eye Hospital
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm 4
Arm 5
Arm Type
Active Comparator
Experimental
Experimental
Experimental
Placebo Comparator
Arm Label
Chlorhexidine monotherapy
Chlorhexidine plus povidone iodine
Early corticosteroids
Late corticosteroids
Placebo
Arm Description
Topical chlorhexidine 0.04%
Topical chlorhexidine 0.04% plus povidone iodine 2.5%
Topical prednisolone sodium phosophate 1% for weeks 4-11
Artificial tears for weeks 4-5, then topical prednisolone sodium phosophate 1% for weeks 6-11
Artificial tears for weeks 4-11
Outcomes
Primary Outcome Measures
Trial 1: Microbial clearance
Acanthamoeba culture
Trial 2: Best spectacle corrected visual acuity
Secondary Outcome Measures
Trial 1: Best spectacle corrected visual acuity
Trial 1: Time to re-epithelialization
Trial 1: Clinical cure
Trial 2: Time to clinical cure
Full Information
NCT ID
NCT03484507
First Posted
March 24, 2018
Last Updated
January 5, 2023
Sponsor
University of California, San Francisco
Collaborators
Research to Prevent Blindness
1. Study Identification
Unique Protocol Identification Number
NCT03484507
Brief Title
Parasitic Ulcer Treatment Trial Pilot
Official Title
Parasitic Ulcer Treatment Trial Pilot
Study Type
Interventional
2. Study Status
Record Verification Date
January 2023
Overall Recruitment Status
Active, not recruiting
Study Start Date
January 1, 2018 (Actual)
Primary Completion Date
December 31, 2023 (Anticipated)
Study Completion Date
December 31, 2023 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of California, San Francisco
Collaborators
Research to Prevent Blindness
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
This is a study of optimal treatments for acanthamoeba keratitis. In the first part of the study, participants will be randomized to chlorhexidine monotherapy or chlorhexidine plus povidone iodine. After four weeks of therapy, participants will be re-randomized to early corticosteroids, later corticosteroids, or placebo.
Detailed Description
Acanthamoeba keratitis is a rare eye infection that is difficult to treat. The mainstay of therapy is a biguanide agent such as chlorhexidine, though recent studies have found povidone iodine to be effective for killing acanthamoeba organisms in vitro. Thus, we randomize participants to topical chlorhexidine 0.04% monotherapy (i.e., routine care) versus topical chlorhexidine 0.04% plus topical poviodine iodine 2.5%. The primary outcome is clearance of acanthamoeba from the ocular surface at 4 weeks.
The role of topical corticosteroids in acanthamoeba keratitis is controversial. Topical corticosteroids can promote growth of acanthamoeba, but may also reduce inflammation and vision-threatening complications of infection. Here, we randomize participants who have completed a course of anti-amoebic therapy to one of three groups: early prednisolone sodium phosphate 1% (started at 4 weeks), late prednisolone sodium phosphate 1% (started at 6 weeks) or placebo (started at 4 weeks). The primary outcome will be visual acuity at 6 months.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Acanthamoeba Keratitis
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderOutcomes Assessor
Allocation
Randomized
Enrollment
49 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Chlorhexidine monotherapy
Arm Type
Active Comparator
Arm Description
Topical chlorhexidine 0.04%
Arm Title
Chlorhexidine plus povidone iodine
Arm Type
Experimental
Arm Description
Topical chlorhexidine 0.04% plus povidone iodine 2.5%
Arm Title
Early corticosteroids
Arm Type
Experimental
Arm Description
Topical prednisolone sodium phosophate 1% for weeks 4-11
Arm Title
Late corticosteroids
Arm Type
Experimental
Arm Description
Artificial tears for weeks 4-5, then topical prednisolone sodium phosophate 1% for weeks 6-11
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Artificial tears for weeks 4-11
Intervention Type
Drug
Intervention Name(s)
Chlorhexidine
Intervention Description
1 drop half-hourly for days 1-2, then hourly for days 3-6, then 8 times daily until the 4-week visit
Intervention Type
Drug
Intervention Name(s)
Povidone-Iodine
Intervention Description
1 drop half-hourly for days 1-2, then hourly for days 3-6, then 8 times daily until the 4-week visit
Intervention Type
Drug
Intervention Name(s)
Prednisolone Sodium Phosphate
Intervention Description
1 drop 4 times daily for weeks 4-9, then 2 times daily for weeks 10-11
Intervention Type
Drug
Intervention Name(s)
Hydroxypropyl Methylcellulose
Intervention Description
1 drop 4 times daily for weeks 4-9, then 2 times daily for weeks 10-11
Intervention Type
Drug
Intervention Name(s)
Prednisolone Sodium Phosphate
Intervention Description
1 drop 4 times daily for weeks 6-9, then 2 times daily for weeks 10-11
Intervention Type
Drug
Intervention Name(s)
Hydroxypropyl Methylcellulose
Intervention Description
1 drop 4 times daily for weeks 4-5
Primary Outcome Measure Information:
Title
Trial 1: Microbial clearance
Description
Acanthamoeba culture
Time Frame
4 weeks
Title
Trial 2: Best spectacle corrected visual acuity
Time Frame
6 months
Secondary Outcome Measure Information:
Title
Trial 1: Best spectacle corrected visual acuity
Time Frame
4 weeks
Title
Trial 1: Time to re-epithelialization
Time Frame
4 weeks
Title
Trial 1: Clinical cure
Time Frame
4 weeks
Title
Trial 2: Time to clinical cure
Time Frame
6 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
13 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Trial 1 Inclusion Criteria:
Smear or culture positive for acanthamoeba
Age 13 years or greater
Trial 1 Exclusion Criteria:
Interstitial or viral keratitis on history or examination
Corneal perforation
Therapeutic keratoplasty for acanthamoeba keratitis
Unwillingness or inability to follow-up (e.g., living too far from hospital)
Trial 2 Inclusion Criteria
Smear or culture positive for acanthamoeba, with 4 weeks of anti-amoebic treatment
Age 13 years or greater
Willing to participate in study
Trial 2 Exclusion Criteria
Interstitial or viral keratitis on history or examination
Fungus identified on culture and smear after 2 weeks of anti-amoebic treatment
Corneal perforation
Therapeutic keratoplasty for acanthamoeba keratitis
Unwillingness or inability to follow-up (e.g., living too far from hospital)
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jeremy D Keenan, MD
Organizational Affiliation
University of California, San Francisco
Official's Role
Principal Investigator
Facility Information:
Facility Name
Aravind Eye Hospital
City
Coimbatore
State/Province
Tamil Nadu
Country
India
Facility Name
Aravind Eye Hospital
City
Madurai
State/Province
Tamil Nadu
Country
India
12. IPD Sharing Statement
Plan to Share IPD
No
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Parasitic Ulcer Treatment Trial Pilot
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