Clinical Trial of Rifampin and Azithromycin for the Treatment of River Blindness
Primary Purpose
Onchocerciasis
Status
Completed
Phase
Phase 2
Locations
Guatemala
Study Type
Interventional
Intervention
Rifampin
Azithromycin
Sponsored by
About this trial
This is an interventional treatment trial for Onchocerciasis focused on measuring Onchocerciasis, Wolbachia, Therapy
Eligibility Criteria
Inclusion Criteria: Males and non-pregnant/non lactating females >5 years of age One onchocercal nodule in an anatomical position where it can be easily removed surgically Exclusion Criteria: Pregnancy (based on urine pregnancy test) Breast-feeding Women taking oral contraceptives Allergy or other adverse reaction to either medication Use of other medications that might interact with rifampin Clinical evidence of liver disease (jaundice, swollen abdomen) Clinical evidence of chronic disease/alcoholism
Sites / Locations
- Universidad del Valle/MERTU
Outcomes
Primary Outcome Measures
Eliminating Wolbachia endobacteria present in O. volvulus worms after 9 months
Secondary Outcome Measures
Elimination of microfilaria in skin snips and histological examination of worms after 9 months
Full Information
NCT ID
NCT00127504
First Posted
August 4, 2005
Last Updated
August 23, 2005
Sponsor
Centers for Disease Control and Prevention
Collaborators
Universidad del Valle, Guatemala, University of Alabama at Birmingham
1. Study Identification
Unique Protocol Identification Number
NCT00127504
Brief Title
Clinical Trial of Rifampin and Azithromycin for the Treatment of River Blindness
Official Title
Trial of Rifampin and Azithromycin for Treatment of Endosymbiotic Bacteria (Wolbachia) in Onchocerca Volvulus in Guatemala
Study Type
Interventional
2. Study Status
Record Verification Date
August 2005
Overall Recruitment Status
Completed
Study Start Date
July 2003 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
May 2004 (undefined)
3. Sponsor/Collaborators
Name of the Sponsor
Centers for Disease Control and Prevention
Collaborators
Universidad del Valle, Guatemala, University of Alabama at Birmingham
4. Oversight
5. Study Description
Brief Summary
The purpose of this study is to determine whether rifampin and/or azithromycin are effective in the treatment of river blindness (onchocerciasis).
Detailed Description
Mass treatment with ivermectin (Mectizan, Merck & Co) is the mainstay of the current efforts to control onchocerciasis, but the drug is not lethal to adult Onchocerca volvulus parasites. Wolbachia, an endosymbiotic bacterium necessary for the fecundity of O. volvulus, can be eradicated with four-six week courses of doxycycline, but this cannot be implemented in current mass drug administration programs. The purpose of this study is to evaluate if a shorter course (five days) with antibiotics that could be used in children and potentially pregnant women would likewise be effective.
Guatemalan patients with onchocercal nodules will be enrolled in an open label trial with four treatment groups: Group A (rifampin 20 mg/kg by mouth [po; maximum 600 mg/day]); B (azithromycin 12 mg/kg po [maximum 500 mg/day]); C (combination of rifampin 20 mg/kg po [maximum 600 mg/day] and azithromycin 12 mg/kg po [maximum 500 mg/day]); D (control group, multivitamin). At the end of the five day treatment course all participants will receive a single dose of ivermectin (150 mcg/kg).
Nodulectomies will be performed 9 months after treatment and the O. volvulus will be analyzed by immunohistochemical staining specific for Wolbachia.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Onchocerciasis
Keywords
Onchocerciasis, Wolbachia, Therapy
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
80 (false)
8. Arms, Groups, and Interventions
Intervention Type
Drug
Intervention Name(s)
Rifampin
Intervention Type
Drug
Intervention Name(s)
Azithromycin
Primary Outcome Measure Information:
Title
Eliminating Wolbachia endobacteria present in O. volvulus worms after 9 months
Secondary Outcome Measure Information:
Title
Elimination of microfilaria in skin snips and histological examination of worms after 9 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
5 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Males and non-pregnant/non lactating females >5 years of age
One onchocercal nodule in an anatomical position where it can be easily removed surgically
Exclusion Criteria:
Pregnancy (based on urine pregnancy test)
Breast-feeding
Women taking oral contraceptives
Allergy or other adverse reaction to either medication
Use of other medications that might interact with rifampin
Clinical evidence of liver disease (jaundice, swollen abdomen)
Clinical evidence of chronic disease/alcoholism
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Josef Amann, MD, MPH
Organizational Affiliation
CDC/NCID/DPD
Official's Role
Principal Investigator
Facility Information:
Facility Name
Universidad del Valle/MERTU
City
Guatemala City
Country
Guatemala
12. IPD Sharing Statement
Learn more about this trial
Clinical Trial of Rifampin and Azithromycin for the Treatment of River Blindness
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