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Clinical Trial of Rifampin and Azithromycin for the Treatment of River Blindness

Trial of Rifampin and Azithromycin for Treatment of Endosymbiotic Bacteria (Wolbachia) in Onchocerca Volvulus in Guatemala

Status
Completed
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00127504
Enrollment
80
Registered
2005-08-08
Start date
2003-07-31
Completion date
2004-05-31
Last updated
2024-08-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Onchocerciasis

Keywords

Onchocerciasis, Wolbachia, Therapy

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.

Interventions

DRUGRifampin
DRUGAzithromycin

Sponsors

Universidad del Valle, Guatemala
CollaboratorOTHER
University of Alabama at Birmingham
CollaboratorOTHER
Centers for Disease Control and Prevention
Lead SponsorFED

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
5 Years to No maximum
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frame
Eliminating Wolbachia endobacteria present in O. volvulus worms after 9 months

Secondary

MeasureTime frame
Elimination of microfilaria in skin snips and histological examination of worms after 9 months

Countries

Guatemala

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026