Ocular Changes After Ivermectin - (DOLF IVM/Oncho)
Primary Purpose
Onchocerciasis
Status
Completed
Phase
Not Applicable
Locations
Ghana
Study Type
Interventional
Intervention
Ivermectin 3Mg Tab
Sponsored by
About this trial
This is an interventional other trial for Onchocerciasis focused on measuring mass drug administration, ophthalmology
Eligibility Criteria
Inclusion Criteria:
- Have at least 1 palpable subcutaneous nodule (onchocercoma) and ≥ 1 Mf/mg of skin (by skin snip)
Exclusion Criteria:
- Pregnancy and breastfeeding mothers within 1 month of giving birth
- Have base line eye diseases including glaucoma, uveitis, severe keratitis, and/or cataracts that interfere with visualization of the posterior segment of the eye.
- Prior allergic / hypersensitivity reactions or intolerance to ivermectin
- Treatment with ivermectin in the past 6 (six) months
Sites / Locations
- University of Health and Allied Sciences
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Ivermectin
Arm Description
Single dose directly observed treatment with Ivermectin 3Mg Tab (150 ug/kg) delivered orally.
Outcomes
Primary Outcome Measures
Number of participants with complete microfilaria clearance from the eye at 3 months
Microfilaria in the anterior chamber of the eye will be counted during slit lamp examination at time of assessment. Participants without Mf in the eye will be considered clear of infection in the eye.
Number of participants with complete microfilaria clearance from the eye at 6 months
Microfilaria in the anterior chamber of the eye will be counted during slit lamp examination at time of assessment. Participants without Mf in the eye will be considered clear of infection in the eye.
Secondary Outcome Measures
The change from baseline in the number of microfilaria detected in the skin at 3 months
Microfilaria (Mf) in the skin will be detected by skin snip microscopy. Up to four (4) skin snips using a corneoscleral punch will be weighed on an analytical balance and incubated for at least 8 hours in isotonic saline in a well of a flat-bottomed microtitre plate at ambient temperature. The Mf that have emerged will be counted using a microscope. Mf number and skin snip weight will be recorded. The mean skin microfilarial density will be calculated and recorded as mf/mg.
The change from baseline in the number of microfilaria detected in the skin at 6 months
Microfilaria (Mf) in the skin will be detected by skin snip microscopy. Up to four (4) skin snips using a corneoscleral punch will be weighed on an analytical balance and incubated for at least 8 hours in isotonic saline in a well of a flat-bottomed microtitre plate at ambient temperature. The Mf that have emerged will be counted using a microscope. Mf number and skin snip weight will be recorded. The mean skin microfilarial density will be calculated and recorded as mf/mg.
The change from baseline in the number of microfilaria detected in the eye at 3 months
Microfilaria in the anterior chamber of the eye will be counted during slit lamp examination at time of assessment.
The change from baseline in the number of microfilaria detected in the eye at 6 months
Microfilaria in the anterior chamber of the eye will be counted during slit lamp examination at time of assessment.
Number of participants with complete microfilaria clearance from the skin at 3 months
Microfilaria (Mf) in the skin will be detected by skin snip microscopy. Up to four (4) skin snips using a corneoscleral punch will be weighed on an analytical balance and incubated for at least 8 hours in isotonic saline in a well of a flat-bottomed microtitre plate at ambient temperature. The Mf that have emerged will be counted using a microscope. Mf number and skin snip weight will be recorded. Participants without Mf in the skin will be considered clear of infection in the skin.
Number of participants with complete microfilaria clearance from the skin at 6 months
Microfilaria (Mf) in the skin will be detected by skin snip microscopy. Up to four (4) skin snips using a corneoscleral punch will be weighed on an analytical balance and incubated for at least 8 hours in isotonic saline in a well of a flat-bottomed microtitre plate at ambient temperature. The Mf that have emerged will be counted using a microscope. Mf number and skin snip weight will be recorded. Participants without Mf in the skin will be considered clear of infection in the skin.
Full Information
NCT ID
NCT03517462
First Posted
April 23, 2018
Last Updated
December 30, 2020
Sponsor
Washington University School of Medicine
Collaborators
Case Western Reserve University, University of Health and Allied Sciences
1. Study Identification
Unique Protocol Identification Number
NCT03517462
Brief Title
Ocular Changes After Ivermectin - (DOLF IVM/Oncho)
Official Title
Microfilarial Clearance From the Eye and Ocular Changes Associated With Ivermectin Treatment in Individuals With Onchocerciasis
Study Type
Interventional
2. Study Status
Record Verification Date
December 2020
Overall Recruitment Status
Completed
Study Start Date
August 6, 2018 (Actual)
Primary Completion Date
August 23, 2019 (Actual)
Study Completion Date
August 23, 2019 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Washington University School of Medicine
Collaborators
Case Western Reserve University, University of Health and Allied Sciences
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
The DOLF Ocular Changes after Ivermectin study will investigate the kinetics of O. volvulus microfilaria (Mf) in the eye following treatment with ivermectin. The primary objective is to determine the proportion of participants with complete Mf clearance from the eye at 3 and 6 months following treatment with ivermectin (IVM).
Detailed Description
This study will examine the kinetics of Mf clearance in the eye following ivermectin treatment. Previous studies have been unable to fully assess clearance Mf from the posterior chamber of the eye. This study will be the first to use optical coherence tomography (OCT) in patients with onchocerciasis to document parasites and pathology in the anterior and posterior chambers of the eye, and assess ocular changes following standard ivermectin treatment.
This will be a biomedical prospective cohort study.
The cohort will be stratified based on Mf levels to achieve approximately the following distribution of individuals with roughly one-third of participants in each group.
Individuals with positive skin snip Mf density of ≥ 1 Mf/mg), but no observable Mf in eyes using slit lamp and indirect ophthalmoscopy
Individuals with positive skin snip Mf density of ≥ 1 Mf/mg and 1-10 Mf in either eye at baseline (based on the highest number counted in either eye)
Individuals with positive skin snip Mf density of ≥ 1 Mf/mg and >10 Mf in either eye at baseline.
All participants recruited into the study will be treated with a single dose of ivermectin (150 ug/kg) by mouth under direct observation. This is the standard of care for treatment with onchocerciasis.
Participants will be evaluated following treatment with detailed parasitological and ocular examinations 7 days, 3 months and 6 months after treatment.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Onchocerciasis
Keywords
mass drug administration, ophthalmology
7. Study Design
Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Model Description
Participants are all given a standard treatment (ivermectin) for onchocerciasis.
Masking
None (Open Label)
Allocation
N/A
Enrollment
231 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Ivermectin
Arm Type
Experimental
Arm Description
Single dose directly observed treatment with Ivermectin 3Mg Tab (150 ug/kg) delivered orally.
Intervention Type
Drug
Intervention Name(s)
Ivermectin 3Mg Tab
Intervention Description
ivermectin tablet
Primary Outcome Measure Information:
Title
Number of participants with complete microfilaria clearance from the eye at 3 months
Description
Microfilaria in the anterior chamber of the eye will be counted during slit lamp examination at time of assessment. Participants without Mf in the eye will be considered clear of infection in the eye.
Time Frame
3 months following treatment
Title
Number of participants with complete microfilaria clearance from the eye at 6 months
Description
Microfilaria in the anterior chamber of the eye will be counted during slit lamp examination at time of assessment. Participants without Mf in the eye will be considered clear of infection in the eye.
Time Frame
6 months following treatment
Secondary Outcome Measure Information:
Title
The change from baseline in the number of microfilaria detected in the skin at 3 months
Description
Microfilaria (Mf) in the skin will be detected by skin snip microscopy. Up to four (4) skin snips using a corneoscleral punch will be weighed on an analytical balance and incubated for at least 8 hours in isotonic saline in a well of a flat-bottomed microtitre plate at ambient temperature. The Mf that have emerged will be counted using a microscope. Mf number and skin snip weight will be recorded. The mean skin microfilarial density will be calculated and recorded as mf/mg.
Time Frame
baseline, and 3 months following treatment
Title
The change from baseline in the number of microfilaria detected in the skin at 6 months
Description
Microfilaria (Mf) in the skin will be detected by skin snip microscopy. Up to four (4) skin snips using a corneoscleral punch will be weighed on an analytical balance and incubated for at least 8 hours in isotonic saline in a well of a flat-bottomed microtitre plate at ambient temperature. The Mf that have emerged will be counted using a microscope. Mf number and skin snip weight will be recorded. The mean skin microfilarial density will be calculated and recorded as mf/mg.
Time Frame
baseline, and 6 months following treatment
Title
The change from baseline in the number of microfilaria detected in the eye at 3 months
Description
Microfilaria in the anterior chamber of the eye will be counted during slit lamp examination at time of assessment.
Time Frame
baseline, 3 months following treatment
Title
The change from baseline in the number of microfilaria detected in the eye at 6 months
Description
Microfilaria in the anterior chamber of the eye will be counted during slit lamp examination at time of assessment.
Time Frame
baseline, 6 months following treatment
Title
Number of participants with complete microfilaria clearance from the skin at 3 months
Description
Microfilaria (Mf) in the skin will be detected by skin snip microscopy. Up to four (4) skin snips using a corneoscleral punch will be weighed on an analytical balance and incubated for at least 8 hours in isotonic saline in a well of a flat-bottomed microtitre plate at ambient temperature. The Mf that have emerged will be counted using a microscope. Mf number and skin snip weight will be recorded. Participants without Mf in the skin will be considered clear of infection in the skin.
Time Frame
3 months following treatment
Title
Number of participants with complete microfilaria clearance from the skin at 6 months
Description
Microfilaria (Mf) in the skin will be detected by skin snip microscopy. Up to four (4) skin snips using a corneoscleral punch will be weighed on an analytical balance and incubated for at least 8 hours in isotonic saline in a well of a flat-bottomed microtitre plate at ambient temperature. The Mf that have emerged will be counted using a microscope. Mf number and skin snip weight will be recorded. Participants without Mf in the skin will be considered clear of infection in the skin.
Time Frame
6 months following treatment
Other Pre-specified Outcome Measures:
Title
Assess the utility of optical coherence tomography for evaluating the presence and clearance of Mf in the anterior and posterior segments of the eye.
Description
Results from the optical coherence tomography (OCT) will be compared with slit lamp and other ocular examinations
Time Frame
baseline, 3 and 6 months following treatment
Title
Evaluate ocular changes between baseline and 3 months following ivermectin treatment using OCT
Description
Results from the optical coherence tomography (OCT) will be compared in participants pre and post treatment
Time Frame
baseline, and 3 months following treatment
Title
Evaluate ocular changes between baseline and 6 months following ivermectin treatment using OCT
Description
Results from the optical coherence tomography (OCT) will be compared in participants pre and post treatment
Time Frame
baseline, and 6 months following treatment
10. Eligibility
Sex
All
Minimum Age & Unit of Time
16 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Have at least 1 palpable subcutaneous nodule (onchocercoma) and ≥ 1 Mf/mg of skin (by skin snip)
Exclusion Criteria:
Pregnancy and breastfeeding mothers within 1 month of giving birth
Have base line eye diseases including glaucoma, uveitis, severe keratitis, and/or cataracts that interfere with visualization of the posterior segment of the eye.
Prior allergic / hypersensitivity reactions or intolerance to ivermectin
Treatment with ivermectin in the past 6 (six) months
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Gary Weil, MD
Organizational Affiliation
Washington University School of Medicine
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Christopher King, MD PhD
Organizational Affiliation
Case Western Reserve University
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Health and Allied Sciences
City
Hohoe
Country
Ghana
12. IPD Sharing Statement
Plan to Share IPD
Yes
IPD Sharing Plan Description
Datasets used for published results will be shared publically through a journal or other open source data repository so that the broader scientific community can access it. Only de-identified data will be shared publicly.
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Ocular Changes After Ivermectin - (DOLF IVM/Oncho)
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