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Twice Yearly Treatment for the Control of LF

Primary Purpose

Lymphatic Filariasis, Helminth Infection

Status
Completed
Phase
Phase 4
Locations
Ghana
Study Type
Interventional
Intervention
400 μg/kg Ivermectin + 400 mg Albendazole
Sponsored by
Noguchi Memorial Institute for Medical Research
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Lymphatic Filariasis focused on measuring Twice a year treatment, Biannual treatment, Wuchereria bancrofti

Eligibility Criteria

5 Years - undefined (Child, Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Residency in the disease endemic community for at least 12 months
  • Willingness to provide informed consent/assent
  • Willingness to donate blood (per the protocol)

Exclusion Criteria:

  • Recent residents (<12 months)
  • Inability to give informed consent
  • Pregnant and lactating women
  • Children below the age of 5.

Sites / Locations

  • Noguchi Memorial Institute for Medical Research

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

Control group

Expanded frequency group

Arm Description

400 μg/kg Ivermectin + 400 mg Albendazole Tablets given every year for 2 years

400 μg/kg Ivermectin + 400 mg Albendazole, Tablets given every 6 months for 2 years

Outcomes

Primary Outcome Measures

Change from baseline prevalence of Lymphatic Filariasis at 24 months
The primary outcome, the prevalence of LF infection, will be measured through cross-sectional parasitological surveys conducted at baseline and at 24 months. The timing of the final follow-up survey will take into account differences in time since treatment of the annual and biannual treatment groups at 24 months

Secondary Outcome Measures

Longitudinal assessment of transmission dynamics of Lymphatic Filariasis for modelling the impact of treatment
For the secondary outcome, a subsample of individuals from the clusters in each of the study groups will be followed longitudinally for two and half years, in order to better understand the transmission dynamics of LF and to estimate key parameters for mathematical modelling of transmission dynamics and treatment impact.
Evaluation of community acceptability of twice-yearly treatment, through questionnaires and focus group discussions
A process evaluation, using semi-structured interviews, focus group discussions (FGDs) and a stakeholder analysis, will investigate the community acceptability of the twice-yearly drug administration.
Feasibility of scale-up of twice-yearly treatment, through questionnaires and focus group discussions
A process evaluation, using semi-structured interviews, focus group discussions (FGDs) and a stakeholder analysis, will investigate the feasibility of scaling up the twice-yearly drug administration.

Full Information

First Posted
November 3, 2016
Last Updated
February 25, 2020
Sponsor
Noguchi Memorial Institute for Medical Research
Collaborators
Ghana Health Services
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1. Study Identification

Unique Protocol Identification Number
NCT03036059
Brief Title
Twice Yearly Treatment for the Control of LF
Official Title
Cluster Randomized Community-based Trial of Annual Versus Biannual Single-dose Ivermectin Plus Albendazole Against Wuchereria Bancrofti Infection in Human and Mosquito Populations
Study Type
Interventional

2. Study Status

Record Verification Date
March 2018
Overall Recruitment Status
Completed
Study Start Date
May 19, 2017 (Actual)
Primary Completion Date
December 8, 2019 (Actual)
Study Completion Date
December 8, 2019 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Noguchi Memorial Institute for Medical Research
Collaborators
Ghana Health Services

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
The Global Program for the Elimination of Lymphatic Filariasis (GPELF) has been in operation sing the year 2000, with the aim of eliminating the disease by the year 2020, following 5-6 rounds of effective annual Mass Drug Administration (MDA). The treatment regimen is Ivermectin (IVM) in combination with Diethylcarbamazine (DEC) or Albendazole (ALB). In Ghana, MDA has been undertaken since 2001. While the disease has been eliminated in many areas, transmission has persisted in some implementation units that had experienced 15 or more rounds of MDA. Alternative intervention strategies, including twice yearly MDA and sleeping under insecticidal nets have significantly accelerated transmission interruption in some settings of high transmission intensity. Thus, it is evident that new intervention strategies could eliminate residual infection in areas of persistent transmission and speed up the LF elimination process. This study therefore seeks to test the hypothesis that biannual treatment of LF endemic communities will accelerate interruption of LF transmission. Two cluster randomized trials will be implemented in LF endemic communities in Ghana. The interventions will be yearly or twice-yearly MDA delivered to entire endemic communities. Allocation to study group will be by clusters identified using the prevalence of LF. Clusters will be randomised to one of two groups: receiving either (1) annual treatment with IVM+ALB; (2) annual MDA with IVM +ALB, followed by an additional MDA 6 months later. The primary outcome measure is the prevalence of LF infection, assessed by four cross-sectional surveys. Entomological assessments will also be undertaken to evaluate the transmission intensity of the disease in the study clusters. Costs and cost-effectiveness will be evaluated. Among a random subsample of participants, microfilaria prevalence will be assessed longitudinally. A nested process evaluation, using semi-structured interviews, focus group discussions and a stakeholder analysis, will investigate the community acceptability, feasibility and scale-up of each delivery system.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Lymphatic Filariasis, Helminth Infection
Keywords
Twice a year treatment, Biannual treatment, Wuchereria bancrofti

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Masking Description
Open Label
Allocation
Randomized
Enrollment
1462 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Control group
Arm Type
Active Comparator
Arm Description
400 μg/kg Ivermectin + 400 mg Albendazole Tablets given every year for 2 years
Arm Title
Expanded frequency group
Arm Type
Experimental
Arm Description
400 μg/kg Ivermectin + 400 mg Albendazole, Tablets given every 6 months for 2 years
Intervention Type
Drug
Intervention Name(s)
400 μg/kg Ivermectin + 400 mg Albendazole
Other Intervention Name(s)
Mectizan, Stromectol
Intervention Description
400ug/Kg, tablet, given orally once or twice a year.
Primary Outcome Measure Information:
Title
Change from baseline prevalence of Lymphatic Filariasis at 24 months
Description
The primary outcome, the prevalence of LF infection, will be measured through cross-sectional parasitological surveys conducted at baseline and at 24 months. The timing of the final follow-up survey will take into account differences in time since treatment of the annual and biannual treatment groups at 24 months
Time Frame
0 and 24 months
Secondary Outcome Measure Information:
Title
Longitudinal assessment of transmission dynamics of Lymphatic Filariasis for modelling the impact of treatment
Description
For the secondary outcome, a subsample of individuals from the clusters in each of the study groups will be followed longitudinally for two and half years, in order to better understand the transmission dynamics of LF and to estimate key parameters for mathematical modelling of transmission dynamics and treatment impact.
Time Frame
0, 12, 24, 30 months
Title
Evaluation of community acceptability of twice-yearly treatment, through questionnaires and focus group discussions
Description
A process evaluation, using semi-structured interviews, focus group discussions (FGDs) and a stakeholder analysis, will investigate the community acceptability of the twice-yearly drug administration.
Time Frame
24 months
Title
Feasibility of scale-up of twice-yearly treatment, through questionnaires and focus group discussions
Description
A process evaluation, using semi-structured interviews, focus group discussions (FGDs) and a stakeholder analysis, will investigate the feasibility of scaling up the twice-yearly drug administration.
Time Frame
24 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
5 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Residency in the disease endemic community for at least 12 months Willingness to provide informed consent/assent Willingness to donate blood (per the protocol) Exclusion Criteria: Recent residents (<12 months) Inability to give informed consent Pregnant and lactating women Children below the age of 5.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Dziedzom K de Souza, PhD
Organizational Affiliation
Noguchi Memorial Institute for Medical Research
Official's Role
Principal Investigator
Facility Information:
Facility Name
Noguchi Memorial Institute for Medical Research
City
Legon-Accra
Country
Ghana

12. IPD Sharing Statement

Plan to Share IPD
No
IPD Sharing Plan Description
IPD will not be shared publicly. Researchers interested in the data can contact the principal investigator directly. No personal identifying information will be shared.
Citations:
PubMed Identifier
28969715
Citation
de Souza DK, Ahorlu CS, Adu-Amankwah S, Otchere J, Mensah SK, Larbi IA, Mensah GE, Biritwum NK, Boakye DA. Community-based trial of annual versus biannual single-dose ivermectin plus albendazole against Wuchereria bancrofti infection in human and mosquito populations: study protocol for a cluster randomised controlled trial. Trials. 2017 Oct 2;18(1):448. doi: 10.1186/s13063-017-2196-9.
Results Reference
derived

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Twice Yearly Treatment for the Control of LF

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