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Triple Combinations Against Hookworm Infections in Lao (Tricombi)

Primary Purpose

Hookworm Infection

Status
Completed
Phase
Phase 4
Locations
Lao People's Democratic Republic
Study Type
Interventional
Intervention
Albendazole
Pyrantel Pamoate
Oxantel Pamoate
Mebendazole
Sponsored by
Swiss Tropical & Public Health Institute
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Hookworm Infection

Eligibility Criteria

6 Years - 15 Years (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Written informed consent signed by parents and/or legal representative; and a verbal assent (children <12 years) or signed assent (children ≥12 years), according to Lao regulations.
  • Able and willing to be examined by a study physician at the beginning of the study.
  • Able and willing to provide two stool samples at the beginning (baseline) and two to three weeks after treatment (follow-up).
  • Positive for hookworm eggs in the stool.
  • Absence of major systemic illnesses, e.g. diabetes, severe anemia as assessed by a medical doctor, upon initial clinical assessment.
  • No known or reported history of chronical illness as cancer, diabetes, chronic heart, liver or renal disease.
  • No recent anthelminthic treatment (within past 4 weeks).
  • No known allergy to study medications (e.g. albendazole, mebendazole, pyrantel pamoate, oxantel pamoate).
  • Negative pregnancy test (girls ≥12 years)

Exclusion Criteria:

  • No written informed consent by parents and/or legal representative and no verbal assent (children <12 years) or signed assent (children ≥12 years).
  • Presence of major systemic illnesses, e.g. diabetes, severe anemia as assessed by a medical doctor, upon initial clinical assessment.
  • History of acute or severe chronic disease.
  • Recent use of anthelminthic drug (within past 4 weeks).
  • Attending other clinical trials during the study.
  • Negative diagnostic result for hookworm eggs in the stool.
  • Positive pregnancy test (girls ≥12 years)

Sites / Locations

  • Nambak District Hospital

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Active Comparator

Experimental

Experimental

Experimental

Arm Label

Albendazole triple combi

Pyrantel pamoate double combi

Albendazole double combi

Mebendazole triple combi

Arm Description

Albendazole (400 mg) + pyrantel pamoate (20 mg/kg) + oxantel pamoate (20 mg/kg)

Pyrantel pamoate (20 mg/kg) + oxantel pamoate (20 mg/kg)

Albendazole (400 mg) + oxantel pamoate (20 mg/kg)

Mebendazole (500mg) + pyrantel pamoate (20 mg/kg) + oxantel pamoate (20 mg/kg)

Outcomes

Primary Outcome Measures

Cure rates of three drug combinations
to comparatively assess the efficacy (based on cure rates, CR) i) albendazole-oxantel pamoate, ii) pyrantel pamoate-oxantel pamoate, iii) albendazole-pyrantel pamoate-oxantel pamoate in school-aged children infected with hookworms.

Secondary Outcome Measures

Cure rates against hookworm of the two triple combinations
To assess the CRs against hookworm of albendazole-pyrantel pamoate-oxantel pamoate versus mebendazole-pyrantel pamoate-oxantel pamoate (proof of concept)
Egg reduction rates (ERR) against hookworm and ERRs/CRs against A. lumbricoides and T. trichiura
Assessing the egg reduction rates (ERR) against hookworm and ERRs and cure rates (CR) against A. lumbricoides and T. trichiura
Incidence of adverse events 3 and 24 hours after treatment
Participants will be interviewed using a standardized questionnaire, before treatment for clinical symptoms and 3 and 24 hours after treatment about the occurrence of adverse events.

Full Information

First Posted
September 6, 2017
Last Updated
May 7, 2018
Sponsor
Swiss Tropical & Public Health Institute
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1. Study Identification

Unique Protocol Identification Number
NCT03278431
Brief Title
Triple Combinations Against Hookworm Infections in Lao
Acronym
Tricombi
Official Title
Different Drug Combinations Against Hookworm Infection in School-aged Children in the Lao People's Democratic Republic, a Single Blind, Randomised Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
May 2018
Overall Recruitment Status
Completed
Study Start Date
September 27, 2017 (Actual)
Primary Completion Date
November 17, 2017 (Actual)
Study Completion Date
December 1, 2017 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Swiss Tropical & Public Health Institute

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
More than one billion people are infected with soil-transmitted helminths (STH, A. lumbricoides, hookworm or Trichuris trichiura). Preventive chemotherapy - i.e. annual or biannual treatment of at-risk populations with albendazole or mebendazole is the current strategy against STH. However, the efficacy of both drugs is only moderate against hookworm and low against T. trichiura. For increasing the efficacy and to avoid drug resistance, new drugs or the combination of different drugs is the way forward. In this randomised controlled trial, we assess the efficacy (based on cure rates) of different drug combinations in school-aged children in Lao. 420 hookworm positive children will be treated: 140 with albendazole-oxantel pamoate, 140 with albendazole-pyrantel pamoate-oxantel pamoate treatment arms, 70 with pyrantel pamoate-oxantel pamoate and 70 with mebendazole-pyrantel pamoate-oxantel pamoate. Two stool samples will be collected at baseline and follow-up (14-21 days after treatment) and analysed with Kato-Katz.
Detailed Description
More than one billion people are infected with A. lumbricoides, hookworm or Trichuris trichiura, the so-called soil-transmitted helminths (STH). Preventive chemotherapy - i.e. annual or biannual treatment of at-risk populations, is the current strategy against STH advocated by the World Health Organization. However, the currently used drugs albendazole and mebendazole have only moderate efficacy against hookworm and low against T. trichiura. The main challenge is their temporal decrease in efficacy, which might be associated with drug resistance, as it was shown in veterinary medicine. For increasing the efficacy and to avoid drug resistance, new drugs or the combination of different drugs is the way forward. The primary objective of this study is to assess the efficacy (based on cure rates [CR]) of the three combinations, i.e. albendazole-oxantel pamoate, pyrantel pamoate-oxantel pamoate and albendazole-pyrantel pamoate-oxantel pamoate in school-aged children infected with hookworms in Laos. Secondary objectives include; i) a proof of concept, investigating the difference between the two triple combinations albendazole-pyrantel pamoate-oxantel pamoate versus mebendazole-pyrantel pamoate-oxantel pamoate (based on CRs), ii) egg reduction rates (ERR) against hookworm and ERRs/CRs against A. lumbricoides and T. trichiura and iii) tolerability of the 4 combinations. Two stool samples will be collected from school-aged children (age 6-15) at baseline. 420 hookworm positive children will be treated: 140 with albendazole-oxantel pamoate, 140 with albendazole-pyrantel pamoate-oxantel pamoate, 70 with pyrantel pamoate-oxantel pamoate and 70 with mebendazole-pyrantel pamoate-oxantel pamoate treatment arms The medical history of the participating children will be assessed with a standardized questionnaire, in addition to a clinical examination carried out by the study physician on the treatment day. Children will be interviewed before treatment for clinical symptoms and 3 and 24 hours after treatment about the occurrence of adverse events. The efficacy of the treatment will be determined 14-21 days post-treatment by collecting another two stool samples. All stool samples will be examined with duplicated Kato-Katz thick smears.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hookworm Infection

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
Participant
Masking Description
Single-blind
Allocation
Randomized
Enrollment
420 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Albendazole triple combi
Arm Type
Active Comparator
Arm Description
Albendazole (400 mg) + pyrantel pamoate (20 mg/kg) + oxantel pamoate (20 mg/kg)
Arm Title
Pyrantel pamoate double combi
Arm Type
Experimental
Arm Description
Pyrantel pamoate (20 mg/kg) + oxantel pamoate (20 mg/kg)
Arm Title
Albendazole double combi
Arm Type
Experimental
Arm Description
Albendazole (400 mg) + oxantel pamoate (20 mg/kg)
Arm Title
Mebendazole triple combi
Arm Type
Experimental
Arm Description
Mebendazole (500mg) + pyrantel pamoate (20 mg/kg) + oxantel pamoate (20 mg/kg)
Intervention Type
Drug
Intervention Name(s)
Albendazole
Intervention Description
Albendazole (400 mg) from Janssen, donated by the World Health Organization
Intervention Type
Drug
Intervention Name(s)
Pyrantel Pamoate
Intervention Description
Pyrantel pamoate (20 mg/kg), will be purchased by the World Health Organization
Intervention Type
Drug
Intervention Name(s)
Oxantel Pamoate
Intervention Description
Oxantel pamoate (20mg/kg) will be produced by the University of Basel
Intervention Type
Drug
Intervention Name(s)
Mebendazole
Intervention Description
Mebendazole (500 mg) from GlaxoSmithKline, donated by the World Health Organization
Primary Outcome Measure Information:
Title
Cure rates of three drug combinations
Description
to comparatively assess the efficacy (based on cure rates, CR) i) albendazole-oxantel pamoate, ii) pyrantel pamoate-oxantel pamoate, iii) albendazole-pyrantel pamoate-oxantel pamoate in school-aged children infected with hookworms.
Time Frame
14-21 days after treatment
Secondary Outcome Measure Information:
Title
Cure rates against hookworm of the two triple combinations
Description
To assess the CRs against hookworm of albendazole-pyrantel pamoate-oxantel pamoate versus mebendazole-pyrantel pamoate-oxantel pamoate (proof of concept)
Time Frame
14-21 days after treatment
Title
Egg reduction rates (ERR) against hookworm and ERRs/CRs against A. lumbricoides and T. trichiura
Description
Assessing the egg reduction rates (ERR) against hookworm and ERRs and cure rates (CR) against A. lumbricoides and T. trichiura
Time Frame
14-21 days after treatment
Title
Incidence of adverse events 3 and 24 hours after treatment
Description
Participants will be interviewed using a standardized questionnaire, before treatment for clinical symptoms and 3 and 24 hours after treatment about the occurrence of adverse events.
Time Frame
3 and 24 hours after treatment

10. Eligibility

Sex
All
Minimum Age & Unit of Time
6 Years
Maximum Age & Unit of Time
15 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Written informed consent signed by parents and/or legal representative; and a verbal assent (children <12 years) or signed assent (children ≥12 years), according to Lao regulations. Able and willing to be examined by a study physician at the beginning of the study. Able and willing to provide two stool samples at the beginning (baseline) and two to three weeks after treatment (follow-up). Positive for hookworm eggs in the stool. Absence of major systemic illnesses, e.g. diabetes, severe anemia as assessed by a medical doctor, upon initial clinical assessment. No known or reported history of chronical illness as cancer, diabetes, chronic heart, liver or renal disease. No recent anthelminthic treatment (within past 4 weeks). No known allergy to study medications (e.g. albendazole, mebendazole, pyrantel pamoate, oxantel pamoate). Negative pregnancy test (girls ≥12 years) Exclusion Criteria: No written informed consent by parents and/or legal representative and no verbal assent (children <12 years) or signed assent (children ≥12 years). Presence of major systemic illnesses, e.g. diabetes, severe anemia as assessed by a medical doctor, upon initial clinical assessment. History of acute or severe chronic disease. Recent use of anthelminthic drug (within past 4 weeks). Attending other clinical trials during the study. Negative diagnostic result for hookworm eggs in the stool. Positive pregnancy test (girls ≥12 years)
Facility Information:
Facility Name
Nambak District Hospital
City
Luang Prabang
ZIP/Postal Code
0604
Country
Lao People's Democratic Republic

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
29673735
Citation
Moser W, Sayasone S, Xayavong S, Bounheuang B, Puchkov M, Huwyler J, Hattendorf J, Keiser J. Efficacy and tolerability of triple drug therapy with albendazole, pyrantel pamoate, and oxantel pamoate compared with albendazole plus oxantel pamoate, pyrantel pamoate plus oxantel pamoate, and mebendazole plus pyrantel pamoate and oxantel pamoate against hookworm infections in school-aged children in Laos: a randomised, single-blind trial. Lancet Infect Dis. 2018 Jul;18(7):729-737. doi: 10.1016/S1473-3099(18)30220-2. Epub 2018 Apr 16.
Results Reference
derived

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Triple Combinations Against Hookworm Infections in Lao

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