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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
University of California, San Francisco
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Acanthamoeba Keratitis

Eligibility Criteria

13 Years - undefined (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

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

First Posted
March 24, 2018
Last Updated
January 5, 2023
Sponsor
University of California, San Francisco
Collaborators
Research to Prevent Blindness
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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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