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A clinical trial to study the effectiveness of combination of two drugs compared to standard single drug treatment in practice for the clearance of filarial infection from the infected individuals

ALTERNATE CHEMOTHERAPY REGIMENS FOR THE CLEARENCE OF W.BANCROFTI INFECTION:DOUBLE BLIND RCT TO STUDY THE EFFICACY OF DIFFERENT CO-ADMINISTRATION AND SEQUENTIAL ADMINISTRATION

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2012/02/002467
Enrollment
160
Registered
2012-02-29
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: null- Lymphatic filariasis Microfilaria carriers

Interventions

Intervention1: DEC+Albendazole co-administration: DEC 300 mg and Albendazole 400 mg per day given orally as single dose for 12 days, Intervention2: DEC and Albendazole sequential administration: DEC

Sponsors

Indian Council of Medical Research
Lead Sponsor
Vector Control Research Centre
Collaborator

Eligibility

Inclusion criteria

Inclusion criteria: a) Age 18 years and above b) Residing in or around Pondicherry and adjoining Tamilnadu areas. c) with night blood microfilaria counts > 10 mf/ml by membrane filtration. d) No history of treatment for filarial infection for the last two years at least. e) Willing for home visits by the staff of the center. f) Willing to give written informed consent

Exclusion criteria

Exclusion criteria: a) Body weight less than 30 kg. b) Hepatic or renal disease as evidenced by clinical or biochemical abnormalities. c) concurrent illness like hypertension, diabetes mellitus, cardiac conditions and epilepsy requiring chronic medication. d) Psychiatric illness e). Patients under tetracycline or doxycycline therapy or History of de-worming by albendazole or other anti-helminthics during last one year, f). Pregnancy or lactation

Design outcomes

Primary

MeasureTime frame
complete clearance of mf in 80% of the participantsTimepoint: At 13th week (91 days) post therapy

Secondary

MeasureTime frame
Complete clearance Mf and complete clearance of antigen from the infectedTimepoint: a)Complete clearance of Mf by 26 weeks (180 days) post therapy. b) Complete clearance of antigen by 52 weeks (365days) post therapy

Countries

India

Contacts

Public ContactMrs G Vijayalakshmi
rljbritto@gmail.com0413-2279155

Outcome results

None listed

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