Skip to content

Wolbachia endobacteria in filarial infections - exploring their usefulness as targets for novel chemotherapies that are anti-filarial and improve hydrocele

Wolbachia endobacteria in filarial infections - exploring their usefulness as targets for novel chemotherapies that are anti-filarial and improve hydrocele: a randomised double blind placebo-controlled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN19748404
Enrollment
76
Registered
2009-02-13
Start date
2005-12-01
Completion date
Unknown
Last updated
2015-01-13

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

Conditions

Lymphatic filariasis (Wuchereria bancrofti) Infections and Infestations Filariasis

Interventions

Study drugs and treatment regimens: 1. 200 mg/day doxycycline for 6 weeks 2. Placebo for 6 weeks Contact details for Joint Principal Investigators: Professor Ohene Adjei Kwame Nkrumah University of

Sponsors

Volkswagen Foundation (VolkswagenStiftung) (Germany)
Lead Sponsor

Eligibility

Sex/Gender
Male

Inclusion criteria

Inclusion criteria: 1. Men between 18 - 60 years 2. Resident in the village for five years or more 3. Evidence of hydrocele assessed by physical examination and ultrasonography 4. Good general health without any clinical condition requiring long-term medication 5. Minimum body weight 40 kg

Exclusion criteria

Exclusion criteria: 1. Evidence of clinically significant neurological, cardiac, pulmonary, hepatic, rheumatological, or renal disease by history, physical examination, and/or laboratory tests 2. Behavioural, cognitive or psychiatric disease that, in the opinion of the investigator, affects the ability of the volunteer to understand and cooperate with the study protocol 3. Laboratory evidence of liver disease (aspartate aminotransferase [AST] alanine aminotransferase [ALT] and/or gamma-glutamyl transferase (gGT) greater than 1.25 times the upper limit of normal of the testing laboratory) 4. Laboratory evidence of renal disease (serum creatinine greater than 1.25 times of the upper limit of normal of the testing laboratory) 5. Other conditions that, in the opinion of the investigator, would jeopardise the safety or rights of a volunteer participating in the trial or would render the subject unable to comply with the protocol 6. Volunteer has abused alcohol or illicit drugs during the past 6 months by history 7. History of severe allergic reaction or anaphylaxis 8. Intolerance to doxycycline

Design outcomes

Primary

MeasureTime frame
Reduction in size of clinical and sub-clinical hydrocele, measured pre-treatment as well as 12 months and 24 months after the start of drug administration.

Secondary

MeasureTime frame
1. Reduction in the stage of supratesticular dilation of scrotal lymphatic vessels, measured pre-treatment as well as 12 months and 24 months after the start of drug administration 2. Reduction in circulating filarial antigen levels as a measure of macrofilaricidal effect of doxycycline, measured pre-treatment as well as 3 months, 12 months and 24 months after the start of drug administration 3. Change in systemic immune responses, measured pre-treatment as well as 3 months, 12 months and 24 months after the start of drug administration

Countries

Ghana

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 4, 2026