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The Synergistic Effects of Home-management and Intermittent Preventive Treatment of Malaria in Children (KNUST-COMDIS)

Primary Purpose

Malaria

Status
Completed
Phase
Phase 4
Locations
Ghana
Study Type
Interventional
Intervention
Amodiaquine plus Artesunate co-administration
Sponsored by
Kwame Nkrumah University of Science and Technology
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional health services research trial for Malaria

Eligibility Criteria

3 Months - 59 Months (Child)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • A child in the study cohort will be eligible to receive a course of IPTc (active or placebo) if the child has NO fever (a temperature of 37•5o C or above) or history of fever in the last 24 hours. However, fever is only a temporary exclusion criterion. If a child has fever when he/she is due for an IPTc course, treatment will be given for the fever and the IPTc course given one month after the fever has subsided. This interval between treatment of fever episodes and administration of an IPTc course is proposed in order to minimise the risk of overdosing since the same drug is used for both HMM and IPTc.

Exclusion Criteria:

  • A child in the study cohort will not be eligible to receive a course of IPTc if:

    • The child has a clinical condition that may be classified as severe according to IMCI guidelines.
    • The child is known to suffer from chronic disease(s) e.g. sickle cell disease that might adversely affect the interpretation of study results.
    • The mother/caregiver withdraws consent.

Sites / Locations

  • District Health Administration

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

1

2

Arm Description

The Home Management of Malaria (HMM) is a strategy aimed at improving access to prompt and effective antimalarial treatment of all fevers in children under 5 years. Community Drug Distributors (CDD) have been trained and equipped for this task.

An Intermittent Preventive Treatment (IPTc) schedule for asymptomatic pre-school children during high malaria transmission seasons alongside an ongoing Home Management of Malaria programme

Outcomes

Primary Outcome Measures

Incidence rate of clinical episodes of malaria per child per year

Secondary Outcome Measures

Prevalence of peripheral parasitaemia
Prevalence of anaemia
Parasite density (geometric means)
Proportions adhering to strategies
Incidence of adverse drug effects within 7 days after intervention

Full Information

First Posted
October 25, 2007
Last Updated
September 17, 2015
Sponsor
Kwame Nkrumah University of Science and Technology
Collaborators
Department for International Development, United Kingdom, Malaria Consortium, UK, Center for International Health and Development
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1. Study Identification

Unique Protocol Identification Number
NCT00550160
Brief Title
The Synergistic Effects of Home-management and Intermittent Preventive Treatment of Malaria in Children
Acronym
KNUST-COMDIS
Official Title
The Clinical Impact of Seasonal Intermittent Preventive Treatment (IPT) and Home Management of Malaria (HMM) Using AQ+AS in Ghanaian Children Under 5 Years of Age - a Cluster Randomised Placebo Controlled Trial.
Study Type
Interventional

2. Study Status

Record Verification Date
September 2015
Overall Recruitment Status
Completed
Study Start Date
April 2007 (undefined)
Primary Completion Date
May 2008 (Actual)
Study Completion Date
October 2008 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Kwame Nkrumah University of Science and Technology
Collaborators
Department for International Development, United Kingdom, Malaria Consortium, UK, Center for International Health and Development

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
This cluster randomised trial is proposed to assess the clinical impact of adding a seasonal intermittent preventive treatment (IPTc) schedule for children aged 3 -59 months to a home management of malaria (HMM) programme using AQ+AS in Ghana. The study will be conducted in the Kwaso sub district of the Ejisu-Juaben district of Ghana in which 6 communities will be randomised to implement an IPTc schedule alongside the HMM programme or HMM programme alone. The study will run in three phases; a preparatory phase to set up and obtain baseline morbidity data from a cross-sectional survey; an intervention phase and a post intervention phase of cross-sectional survey and data evaluation and dissemination. A cohort of 546 study children randomly selected will receive three full treatment courses of AS+AQ intermittently during the April - Nov 2007 transmission season. Community-based drug distributors (CDDs) will administer all courses of IPTc. The first dose of each course will be directly observed by the CDDs who will educate mothers or caregivers to administer subsequent doses appropriately at home. Follow up visits to homes will be done by CDDs and field supervisors to ascertain adherence and to monitor adverse drug events. The incidence of clinical malaria and other secondary outcomes will be compared with those of another cohort of 546 study children who will not receive IPTc but may be treated under the HMM strategy alone with AS+AQ when necessary during the observation period.

6. Conditions and Keywords

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

7. Study Design

Primary Purpose
Health Services Research
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
1490 (Actual)

8. Arms, Groups, and Interventions

Arm Title
1
Arm Type
Active Comparator
Arm Description
The Home Management of Malaria (HMM) is a strategy aimed at improving access to prompt and effective antimalarial treatment of all fevers in children under 5 years. Community Drug Distributors (CDD) have been trained and equipped for this task.
Arm Title
2
Arm Type
Experimental
Arm Description
An Intermittent Preventive Treatment (IPTc) schedule for asymptomatic pre-school children during high malaria transmission seasons alongside an ongoing Home Management of Malaria programme
Intervention Type
Drug
Intervention Name(s)
Amodiaquine plus Artesunate co-administration
Intervention Description
Under the Home Management of Malaria (HMM) strategy the Community Drug Distributors (CDD) will treat all children under 5 years presented to them with measured fever or a history of fever with AQ plus AS co-administered. Children under 12 months receive 75mg of AQ co-administered with 25mg of AS daily for three days. Children who are 12 to 59 months old receive 150mg of AQ and 50mg of AS co-administered daily for three days. Asymptomatic children under 5 years in the Intermittent Preventive Treatment (IPTc) clusters will receive additional AQ plus AS co-administered during high malaria transmission season. Those under 12 months will receive 75mg of AQ co-administered with 25mg of AS daily for three days; and children who are 12 to 59 months old receive 150mg of AQ and 50mg of AS co-administered daily for three days.
Primary Outcome Measure Information:
Title
Incidence rate of clinical episodes of malaria per child per year
Time Frame
One year
Secondary Outcome Measure Information:
Title
Prevalence of peripheral parasitaemia
Time Frame
One year
Title
Prevalence of anaemia
Time Frame
One year
Title
Parasite density (geometric means)
Time Frame
One year
Title
Proportions adhering to strategies
Time Frame
One year
Title
Incidence of adverse drug effects within 7 days after intervention
Time Frame
One year

10. Eligibility

Sex
All
Minimum Age & Unit of Time
3 Months
Maximum Age & Unit of Time
59 Months
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: A child in the study cohort will be eligible to receive a course of IPTc (active or placebo) if the child has NO fever (a temperature of 37•5o C or above) or history of fever in the last 24 hours. However, fever is only a temporary exclusion criterion. If a child has fever when he/she is due for an IPTc course, treatment will be given for the fever and the IPTc course given one month after the fever has subsided. This interval between treatment of fever episodes and administration of an IPTc course is proposed in order to minimise the risk of overdosing since the same drug is used for both HMM and IPTc. Exclusion Criteria: A child in the study cohort will not be eligible to receive a course of IPTc if: The child has a clinical condition that may be classified as severe according to IMCI guidelines. The child is known to suffer from chronic disease(s) e.g. sickle cell disease that might adversely affect the interpretation of study results. The mother/caregiver withdraws consent.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Harry Tagbor, DrPH
Organizational Affiliation
Department of Community Health, School of Medical Science, Kwame Nkrumah University of Science & Technology
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Edmund Browne, PhD
Organizational Affiliation
Department of Community Health, School of Medical Sciences, Kwame Nkrumah University of Science & Technology
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Helen Counihan, PhD
Organizational Affiliation
Malaria Consortium, UK
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Sylvia Meek, PhD
Organizational Affiliation
Malaria Consortium, UK
Official's Role
Principal Investigator
Facility Information:
Facility Name
District Health Administration
City
Ejisu
State/Province
Ashanti Region
Country
Ghana

12. IPD Sharing Statement

Learn more about this trial

The Synergistic Effects of Home-management and Intermittent Preventive Treatment of Malaria in Children

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