ALBvLEV: Efficacy Albendazole and Levamisole Against STH on Unguja

Sponsor
Natural History Museum, United Kingdom (Other)
Overall Status
Completed
CT.gov ID
NCT00659997
Collaborator
Ministry of Health, Tanzania (Other), University of London (Other)
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Study Details

Study Description

Brief Summary

Field epidemiological studies undertaken during 2005 in four village locations in Northern Unguja, Zanzibar examined mothers and their pre-school aged children for helminth infections.

The prevalence of Ascaris lumbricoides was found to have remained relatively high despite community-wide treatment with the mass administration of Albendazole (a WHO recommended de-wormer) in coordination with community vitamin A supplementation.

One hypothesis for this is that the children and mothers had Ascaris infections more tolerant to Albendazole that subsequently failed to clear. It is necessary to compare the present drug efficiency of Albendazole (first-line de-wormer) with Levamisole (second-line de-wormer) on STH infections such patients a case-control setting to shed light on the putative resistance of local Ascaris/Trichuris to albendazole.

In so doing, this should clarify whether there is resistance developing towards Albendazole and have possible implications for introducing combination therapies of Levamisole and Albendazole for first line de-worming mothers and their children in the future.

Condition or Disease Intervention/Treatment Phase
Phase 4

Detailed Description

The study was conducted in 10 villages on Unguja Island representative of urban, semi-urban and rural environments. After liaison with the local Shehia (the elected community leader) mothers and their children aged between 6 months and 5 years old were invited to attend a walk-in mobile clinic. In accordance with WHO sample size recommendations of 30 individuals per site and to cater for drop-out/non-compliance, target enrolment was about 50 mother and child pairs at each study village.

Stool specimens were transported to the Helmtin Control Laboratory Unguja laboratory for visual inspection of stool consistency and presence of blood, after which a single Kato-Katz thick smear (41.7mg) was prepared. Eggs of all STH species were counted by inspection at 100x microscopy and expressed as a tally of eggs per gram (EPG). To ensure consistency of egg counts, slides were read by the same two technicians for each study village.

10 Mother and child pairs found positive for Ascaris and/or Trichuris were randomised, by coin tossing, to receive either a single tablet of ALB (400mg) or an appropriate dose of LEV (2.5 mg/kg). A parasitological follow-up took place 18 days after treatment where a requested stool sample was analyzed by a single Kato-Katz thick smear for assessment of STH clearance. In accordance with WHO's 'no survey without service' all attendees were given an additional ALB tablet.

Study Design

Study Type:
Interventional
Actual Enrollment :
20 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Participant)
Primary Purpose:
Treatment
Official Title:
Longitudinal Study of Efficacy of Standard Albendazole Treatment Versus Levamisole/Pyrantel Pamoate on Soil Transmitted Helminth Infections
Study Start Date :
Jun 1, 2006
Actual Primary Completion Date :
Sep 1, 2006
Actual Study Completion Date :
Sep 1, 2007

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: 1

1 Individuals treated with Albendazole

Drug: Albendazole
Single oral dose of 400mg

Active Comparator: 2

Individuals treated with Levamisole

Drug: Levamisole
Single oral dose of 2.5mg/kg

Outcome Measures

Primary Outcome Measures

  1. Clearance of STH faecal eggs in patient stool [18 days]

Eligibility Criteria

Criteria

Ages Eligible for Study:
1 Year to 45 Years
Sexes Eligible for Study:
Female
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Presently with soil-transmitted helminthiasis
Exclusion Criteria:
  • absence of soil-transmitted helminthiasis

Contacts and Locations

Locations

Site City State Country Postal Code
1 Helminth Control Laboratory Unguja Stone Town Tanzania

Sponsors and Collaborators

  • Natural History Museum, United Kingdom
  • Ministry of Health, Tanzania
  • University of London

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
, ,
ClinicalTrials.gov Identifier:
NCT00659997
Other Study ID Numbers:
  • NHMDEWORMING
First Posted:
Apr 17, 2008
Last Update Posted:
Apr 17, 2008
Last Verified:
Apr 1, 2008
Keywords provided by , ,
Additional relevant MeSH terms:

Study Results

No Results Posted as of Apr 17, 2008