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Study of Azithromycin to Prevent Recurrent Trichiasis Following Surgery in Ethiopia (STAR)

Primary Purpose

Trichiasis

Status
Completed
Phase
Phase 4
Locations
United States
Study Type
Interventional
Intervention
azithromycin
topical tetracycline
Sponsored by
Johns Hopkins University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Trichiasis focused on measuring trichiasis, azithromycin, trichiasis surgery, topical tetracycline

Eligibility Criteria

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

Inclusion Criteria: Presence of trichiasis: no previous report of trichiasis surgery in at least one eye with trichiasis: Agreement by at least one other family member accompanying the patient that, if the patient is randomized to the family-treatment arm, s/he also would be willing to receive antibiotic treatment Age 18 or older Exclusion Criteria: other household members concurrently participating in the trial Self-reported pregnancy Documented allergy to tetracycline Plans to move out of the region within 1 year.

Sites / Locations

  • Johns Hopkins University

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Active Comparator

Active Comparator

Active Comparator

Arm Label

Control

Intervention 1

Intervention 2

Arm Description

topical tetracycline

oral azithromycin, single 1g dose to subject

single oral azithromycin dose to subject and immediate family members

Outcomes

Primary Outcome Measures

Recurrent Trichiasis in Tetracycline and Azithromycin Groups
Recurrence of trichiasis : Clinical assessment was done by looking for one or more eye lashes touching globe or evidence of epilation.
Recurrent Trichiasis Between Two Azithromycin Arms
Recurrence of trichiasis :Clinical assessment for recurrence was done by looking for one or more eye lashes touching globe or evidence of epilation. If there was evidence of epilation or if one or more eye lashes were touching the globe, it was considered as recurrence of trichiasis.

Secondary Outcome Measures

Surgical Failure
The surgery was considered a failure if one or more eye lashes were touching the globe of the eye of the subject.
Adverse Events
At 6 weeks participants/family members were asked about any hospitalization,death,ocular complaints, gastrointestinal illness or other specific illness or any clinic visit within six weeks of receiving surgery.

Full Information

First Posted
July 3, 2006
Last Updated
June 27, 2017
Sponsor
Johns Hopkins University
Collaborators
National Eye Institute (NEI), Project ORBIS
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1. Study Identification

Unique Protocol Identification Number
NCT00347776
Brief Title
Study of Azithromycin to Prevent Recurrent Trichiasis Following Surgery in Ethiopia
Acronym
STAR
Official Title
Trial of Antibiotics to Reduce Recurrent Trichiasis (STAR)
Study Type
Interventional

2. Study Status

Record Verification Date
June 2017
Overall Recruitment Status
Completed
Study Start Date
August 2001 (undefined)
Primary Completion Date
December 2003 (Actual)
Study Completion Date
December 2006 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Johns Hopkins University
Collaborators
National Eye Institute (NEI), Project ORBIS

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Trachoma, an ocular infection caused by C. trachomatis, is the second leading cause of blindness worldwide.Years of repeated infection with C. trachomatis cause the eyelid to scar and contract and ultimately to rotate inward such that eyelashes rub against the eyeball and abrade the cornea (trichiasis). The World Health Organization (WHO) has endorsed a multi-faceted strategy to combat trachoma, which includes surgery to correct trichiasis. Despite this encouraging news, under the best of circumstances the recurrence rate of trichiasis following surgery is disappointingly high. The objective of our project is to conduct a randomized, controlled clinical trial of post-surgical antibiotic treatment, comparing oral azithromycin to topical tetracycline, for trichiasis surgical patients in Ethiopia with the goal of determining the impact of treatment on rates of trichiasis recurrence at one and two years.
Detailed Description
A randomized clinical trial of the effectiveness of a single dose of azithromycin compared to 6 weeks of topical tetracycline, and the added benefit of family-based azithromycin treatment, in preventing recurrence of trichiasis following surgery is proposed. This will provide the evidence base to inform and change the global public health policy and the donation program policy, regarding post-surgical treatment for trichiasis patients and possibly their families. The investigators will determine the impact of three treatment strategies following trichiasis surgery on the rate of trichiasis recurrence in the operated eye at six months and one year. A randomized clinical trial of 1425 trichiasis surgical patients will be conducted in Sodo,Ethiopia. The first group (Control Group) will receive topical tetracycline following surgery; the second group (Intervention Patient Group) will receive oral azithromycin; the third group (Intervention Family Group) will receive oral azithromycin, and all family members resident in the patient's household will also receive oral azithromycin. Data will be collected at baseline (pre-surgery) on ocular status and infection status. Data will be collected at the time of surgery on surgery-related variables and surgical and post-operative complications. Additional data will be collected on any surgical complications and early recurrence at the two-week visit when sutures will be removed. A follow up visit at two months will include data collection on recurrence and presence of ocular infection. Evaluations for trichiasis recurrence will occur again at six months and at one year post-surgery. The latter visit will also include data collection on presence of ocular infection in the surgical case, and ocular infection in household members. Evaluation of the risk of recurrence at six months and one, two, and three years within each group will be completed to determine the benefit of using azithromycin compared to topical tetracycline, and the added benefit of family-based treatment.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Trichiasis
Keywords
trichiasis, azithromycin, trichiasis surgery, topical tetracycline

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
1452 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Control
Arm Type
Active Comparator
Arm Description
topical tetracycline
Arm Title
Intervention 1
Arm Type
Active Comparator
Arm Description
oral azithromycin, single 1g dose to subject
Arm Title
Intervention 2
Arm Type
Active Comparator
Arm Description
single oral azithromycin dose to subject and immediate family members
Intervention Type
Drug
Intervention Name(s)
azithromycin
Other Intervention Name(s)
Zithromax
Intervention Description
oral antibiotic
Intervention Type
Drug
Intervention Name(s)
topical tetracycline
Primary Outcome Measure Information:
Title
Recurrent Trichiasis in Tetracycline and Azithromycin Groups
Description
Recurrence of trichiasis : Clinical assessment was done by looking for one or more eye lashes touching globe or evidence of epilation.
Time Frame
Primary outcome assessed at 2 weeks,1.5 months, 6 months and 12 months post-surgery
Title
Recurrent Trichiasis Between Two Azithromycin Arms
Description
Recurrence of trichiasis :Clinical assessment for recurrence was done by looking for one or more eye lashes touching globe or evidence of epilation. If there was evidence of epilation or if one or more eye lashes were touching the globe, it was considered as recurrence of trichiasis.
Time Frame
Primary outcome assessed at 2 weeks,1.5 months, 6 months and 12 months post-surgery
Secondary Outcome Measure Information:
Title
Surgical Failure
Description
The surgery was considered a failure if one or more eye lashes were touching the globe of the eye of the subject.
Time Frame
6 weeks
Title
Adverse Events
Description
At 6 weeks participants/family members were asked about any hospitalization,death,ocular complaints, gastrointestinal illness or other specific illness or any clinic visit within six weeks of receiving surgery.
Time Frame
6 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Presence of trichiasis: no previous report of trichiasis surgery in at least one eye with trichiasis: Agreement by at least one other family member accompanying the patient that, if the patient is randomized to the family-treatment arm, s/he also would be willing to receive antibiotic treatment Age 18 or older Exclusion Criteria: other household members concurrently participating in the trial Self-reported pregnancy Documented allergy to tetracycline Plans to move out of the region within 1 year.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Sheila K West
Organizational Affiliation
Johns Hopkins University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Johns Hopkins University
City
Baltimore
State/Province
Maryland
ZIP/Postal Code
21205
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
16113353
Citation
Melese M, West ES, Alemayehu W, Munoz B, Worku A, Gaydos CA, West SK. Characteristics of trichiasis patients presenting for surgery in rural Ethiopia. Br J Ophthalmol. 2005 Sep;89(9):1084-8. doi: 10.1136/bjo.2005.066076.
Results Reference
background
PubMed Identifier
16424528
Citation
West ES, Munoz B, Imeru A, Alemayehu W, Melese M, West SK. The association between epilation and corneal opacity among eyes with trachomatous trichiasis. Br J Ophthalmol. 2006 Feb;90(2):171-4. doi: 10.1136/bjo.2005.075390.
Results Reference
background
PubMed Identifier
16033749
Citation
West ES, Alemayehu W, Munoz B, Melese M, Imeru A, West SK. Surgery for Trichiasis, Antibiotics to prevent Recurrence (STAR) Clinical Trial methodology. Ophthalmic Epidemiol. 2005 Aug;12(4):279-86. doi: 10.1080/09286580591005769.
Results Reference
background
PubMed Identifier
16534049
Citation
West SK, West ES, Alemayehu W, Melese M, Munoz B, Imeru A, Worku A, Gaydos C, Meinert CL, Quinn T. Single-dose azithromycin prevents trichiasis recurrence following surgery: randomized trial in Ethiopia. Arch Ophthalmol. 2006 Mar;124(3):309-14. doi: 10.1001/archopht.124.3.309.
Results Reference
result
PubMed Identifier
22159169
Citation
Woreta F, Munoz B, Gower E, Alemayehu W, West SK. Three-year outcomes of the surgery for trichiasis, antibiotics to prevent recurrence trial. Arch Ophthalmol. 2012 Apr;130(4):427-31. doi: 10.1001/archophthalmol.2011.374. Epub 2011 Dec 12.
Results Reference
derived
PubMed Identifier
21051704
Citation
Gower EW, Merbs SL, Munoz BE, Kello AB, Alemayehu W, Imeru A, West SK. Rates and risk factors for unfavorable outcomes 6 weeks after trichiasis surgery. Invest Ophthalmol Vis Sci. 2011 Apr 25;52(5):2704-11. doi: 10.1167/iovs.10-5161. Print 2011 Apr.
Results Reference
derived
PubMed Identifier
19901217
Citation
Woreta TA, Munoz BE, Gower EW, Alemayehu W, West SK. Effect of trichiasis surgery on visual acuity outcomes in Ethiopia. Arch Ophthalmol. 2009 Nov;127(11):1505-10. doi: 10.1001/archophthalmol.2009.278.
Results Reference
derived

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Study of Azithromycin to Prevent Recurrent Trichiasis Following Surgery in Ethiopia

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