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Albendazole Plus High Dose Ivermectin for Trichuriasis in Pediatric Patients (HI4T)

Primary Purpose

Trichuris Infection, Helminthiasis

Status
Completed
Phase
Phase 2
Locations
International
Study Type
Interventional
Intervention
Ivermectin
Albendazole
Sponsored by
Alejandro Krolewiecki
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Trichuris Infection focused on measuring TRICHURIS, STH, IVERMECTIN, ALBENDAZOLE

Eligibility Criteria

2 Years - 14 Years (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Infection with T. trichiura by Kato Katz.
  • Body weight >15kg.
  • Accepts participation

Exclusion Criteria:

  • Albendazole and/or mebendazol treatment in the previous 3 months.
  • Allergy to the study drugs
  • Acute medical conditions
  • Clinical trial participation in the previous 3 months.
  • Pregnancy.

Sites / Locations

  • IIET
  • Universidad Autónoma de Honduras

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Active Comparator

Experimental

Experimental

Experimental

Arm Label

Albendazole 400mg

Albendazole/Ivermectin

Albendazole 400mg x 3

Albendazole/Ivermectin x 3

Arm Description

Albendazole 400mg in single dose

Combination of albendazole 400mg + ivermectin 600mcg/kg in single dose.

Albendazole 400mg/day for 3 consecutive days

Combination of albendazole 400mg/day + ivermectin 600mcg/kg/day for 3 consecutive days

Outcomes

Primary Outcome Measures

Cure Rate
Number of individuals cured from Trichuris trichiura infection using the duplicate Kato Katz laboratory method on a single sample of fresh stools as the measurement tool. Cure rate is defined as the absence of Trichuris trichiura eggs in post-treatment samples.

Secondary Outcome Measures

Egg Change Rate
Calculation details: 100 x (1 - arithmetic mean fecal egg count post-intervention / arithmetic mean fecal egg count pre-intervention) Egg change rate was calculated across all participants, as described in reference: Levecke B et al., PLoS Negl Trop Dis. 2014;8(10).
Beta Tubulin Resistance
Measurement of the incidence of mutations of tubulin in Trichuris trichiura eggs collected pre and post treatment using molecular biology techniques. This data is not available yet due to the COVID-19 pandemic, but the data will be available and reported in the future. Anticipated reporting date for this outcome measure is estimated by 2021 and will be confirmed once the pandemic is over.

Full Information

First Posted
July 22, 2019
Last Updated
July 27, 2020
Sponsor
Alejandro Krolewiecki
Collaborators
Brock University, Universidad Nacional del Centro de la Provincia de Buenos Aires, Universidad Nacional Autonoma de Honduras
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1. Study Identification

Unique Protocol Identification Number
NCT04041453
Brief Title
Albendazole Plus High Dose Ivermectin for Trichuriasis in Pediatric Patients
Acronym
HI4T
Official Title
Prospective, Parallel-group, Open-label Randomized Controlled Trial of Four Treatment Regimes for Trichuriasis in Pediatric Patients
Study Type
Interventional

2. Study Status

Record Verification Date
July 2020
Overall Recruitment Status
Completed
Study Start Date
October 9, 2019 (Actual)
Primary Completion Date
March 7, 2020 (Actual)
Study Completion Date
March 7, 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Alejandro Krolewiecki
Collaborators
Brock University, Universidad Nacional del Centro de la Provincia de Buenos Aires, Universidad Nacional Autonoma de Honduras

4. Oversight

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

5. Study Description

Brief Summary
There are four species of intestinal worms collectively known as soil-transmitted helminthiasis (STH): Ancylostoma duodenale and Necator americanus (hookworms), Ascaris lumbricoides (roundworms), and Trichuris trichiura (whipworms). These parasites affect over two billion people and contribute to significant morbidity and disability, especially in high risk groups, for example children, agricultural workers and pregnant women. In children, STH are associated with impaired nutritional status evidenced by stunting, thinness and underweight. As is the case in most Latin America, STH are a public health problem in Honduras. The World Health Organization (WHO) informs that more than 2.5 million children (under 15 years of age) in the country are at risk of infection. To control these infections Honduras has established a national deworming program that operates since 2001 but despite these efforts, the prevalence of STH infections remains unacceptably high. This is especially true in rural communities where prevalence can be as high as 70% of the children population. Ivermectin (IVM) in combination with albendazole (ALB) has demonstrated the capacity to improve efficacy compared to any of these drugs in monotherapy; the efficacy is however, still inadequate in terms of cure rate, although egg reduction rates are significant. The purpose of the current trial is to assess the safety and efficacy of 3 experimental regimens for the treatment of infections by Trichuris trichiura in children in comparison with the current standard of practice in Mass Drug Administration (MDA) campaigns. The experimental regimens will explore the effect of multiple day regimens and high dose ivermectin. Treatment arms: Group 1: single dose of ALB 400 mg. (active control arm). N:39 Group 2: single dose ALB 400mg + IVM 600µg/Kg. N: 57 Group 3: daily dose ALB 400mg for 3 consecutive days. N:24 Group 4: daily dose ALB 400mg + IVM 600µg for 3 consecutive days. N:57 Total Study Population: 177

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Trichuris Infection, Helminthiasis
Keywords
TRICHURIS, STH, IVERMECTIN, ALBENDAZOLE

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
176 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Albendazole 400mg
Arm Type
Active Comparator
Arm Description
Albendazole 400mg in single dose
Arm Title
Albendazole/Ivermectin
Arm Type
Experimental
Arm Description
Combination of albendazole 400mg + ivermectin 600mcg/kg in single dose.
Arm Title
Albendazole 400mg x 3
Arm Type
Experimental
Arm Description
Albendazole 400mg/day for 3 consecutive days
Arm Title
Albendazole/Ivermectin x 3
Arm Type
Experimental
Arm Description
Combination of albendazole 400mg/day + ivermectin 600mcg/kg/day for 3 consecutive days
Intervention Type
Drug
Intervention Name(s)
Ivermectin
Intervention Description
Ivermectin at 600mcg/kg in addition to albendazole will be provided for 1 or 3 days.
Intervention Type
Drug
Intervention Name(s)
Albendazole
Intervention Description
Albendazole will be provided as an active control or in experimental arms for 1 or 3 days with ivermectin.
Primary Outcome Measure Information:
Title
Cure Rate
Description
Number of individuals cured from Trichuris trichiura infection using the duplicate Kato Katz laboratory method on a single sample of fresh stools as the measurement tool. Cure rate is defined as the absence of Trichuris trichiura eggs in post-treatment samples.
Time Frame
21 days
Secondary Outcome Measure Information:
Title
Egg Change Rate
Description
Calculation details: 100 x (1 - arithmetic mean fecal egg count post-intervention / arithmetic mean fecal egg count pre-intervention) Egg change rate was calculated across all participants, as described in reference: Levecke B et al., PLoS Negl Trop Dis. 2014;8(10).
Time Frame
21 days
Title
Beta Tubulin Resistance
Description
Measurement of the incidence of mutations of tubulin in Trichuris trichiura eggs collected pre and post treatment using molecular biology techniques. This data is not available yet due to the COVID-19 pandemic, but the data will be available and reported in the future. Anticipated reporting date for this outcome measure is estimated by 2021 and will be confirmed once the pandemic is over.
Time Frame
21days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
2 Years
Maximum Age & Unit of Time
14 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Infection with T. trichiura by Kato Katz. Body weight >15kg. Accepts participation Exclusion Criteria: Albendazole and/or mebendazol treatment in the previous 3 months. Allergy to the study drugs Acute medical conditions Clinical trial participation in the previous 3 months. Pregnancy.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Alejandro J Krolewiecki, MD, PhD
Organizational Affiliation
IIET - Universidad Nacional de Salta
Official's Role
Study Director
Facility Information:
Facility Name
IIET
City
Oran
State/Province
Salta
ZIP/Postal Code
4530
Country
Argentina
Facility Name
Universidad Autónoma de Honduras
City
Tegucigalpa
Country
Honduras

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
All IPD that underlie results in a publication.
IPD Sharing Time Frame
After study data analysis completion, with submission for publication to a peer review journal..
IPD Sharing Access Criteria
Database will be made available through a publication.
Citations:
PubMed Identifier
33906234
Citation
Matamoros G, Sanchez A, Gabrie JA, Juarez M, Ceballos L, Escalada A, Rodriguez C, Marti-Soler H, Rueda MM, Canales M, Lanusse C, Cajal P, Alvarez L, Cimino RO, Krolewiecki A. Efficacy and Safety of Albendazole and High-Dose Ivermectin Coadministration in School-Aged Children Infected With Trichuris trichiura in Honduras: A Randomized Controlled Trial. Clin Infect Dis. 2021 Oct 5;73(7):1203-1210. doi: 10.1093/cid/ciab365.
Results Reference
derived

Learn more about this trial

Albendazole Plus High Dose Ivermectin for Trichuriasis in Pediatric Patients

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