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Trial of Malaria Seasonal IPTc Combined With Community Case Management

Primary Purpose

Malaria

Status
Completed
Phase
Phase 3
Locations
Senegal
Study Type
Interventional
Intervention
IPTc+CCM
Community Case Management with artemether-lumefantrine (AL)
Sponsored by
Cheikh Anta Diop University, Senegal
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Malaria focused on measuring IPTc, Community Case Management, Home Management for malaria

Eligibility Criteria

3 Months - 10 Years (Child)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • age between 3 to 120 months
  • consent participation given by parents or guardians
  • willing to remain in the study area in the next 6 months

Exclusion Criteria:

  • Known allergy to the study investigational drug
  • Any underlying chronic or severe condition.
  • Participant under Treatment with sulfamides

Sites / Locations

  • University Cheikh Anta Diop

Arms of the Study

Arm 1

Arm 2

Arm Type

Placebo Comparator

Experimental

Arm Label

Community Case Management

Community Case Management plus IPTc

Arm Description

Provision of access to prompt diagnosis and treatment for malaria by community volunteers in the village (PECADOM)

Monthly Intermittent Preventive Treatment with sulfadoxine pyrimethamine plus amodiaquine, in addition to community case management

Outcomes

Primary Outcome Measures

Number of children under 10 years of age with clinical malaria
children under 10 years age presenting symptoms of malaria with fever (or history of fever in the previous 48 hours) with a positive Rapid Diagnostic Test or positive blood slides

Secondary Outcome Measures

Number of children under 10 years of age presenting clinical Malaria with high parasite density
Malaria with parasite density at 3000 parasites/uL or more in the presence of fever or history of fever in the previous 48hours in children under 10 years of age

Full Information

First Posted
September 11, 2011
Last Updated
April 25, 2012
Sponsor
Cheikh Anta Diop University, Senegal
Collaborators
London School of Hygiene and Tropical Medicine
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1. Study Identification

Unique Protocol Identification Number
NCT01449045
Brief Title
Trial of Malaria Seasonal IPTc Combined With Community Case Management
Official Title
Cluster Randomized Trial of Malaria Seasonal IPTc Combined With Community Case Management in Saraya District, SE Senegal
Study Type
Interventional

2. Study Status

Record Verification Date
April 2012
Overall Recruitment Status
Completed
Study Start Date
July 2011 (undefined)
Primary Completion Date
December 2011 (Actual)
Study Completion Date
February 2012 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Cheikh Anta Diop University, Senegal
Collaborators
London School of Hygiene and Tropical Medicine

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Malaria is a major public health problem. 250 million cases annually leads to approximately 1 million deaths. Over 80 per cent of these deaths occur among African children under age five. The main interventions covered treatment with Artemisinin Combination Therapies (ACT), long lasting bednets distribution and Rapid Diagnosis Tests (RDT) to improve malaria diagnosis. This has led in Senegal to a substantial decrease in the incidence of malaria, in 2009. However the recent overall decline hides the fact that malaria incidence remains very high in the south of Senegal. That's why Home-based management (HMM) for malaria is being introduced in selected areas. Intermittent Preventive Treatment (IPT) by monthly administration of a therapeutic dose of antimalarials can achieve a very high degree of protection from attacks of clinical malaria in children. The purpose of this project is to evaluate the effectiveness of combining IPTc with HMM in southern Senegal The study objectives are to : Assess the tolerance of IPTc using SP+AQ when it is administered for a longer period in areas with a longer transmission season, Assess the added benefit that IPT with the association of Sulfadoxine-Pyrimethamine + Amodiaquine can offer in populations where a rapid and early care with home management of malaria is already established. Determine the cost benefit ratio of the addition of IPTc with HMM. A cluster randomized controlled trial has been designed to evaluate the effectiveness of adding seasonal IPTc with sulfadoxine-pyrimethamine plus amodiaquine (SP+AQ) for 5 months per year, in villages where home-based management of malaria is implemented. All villages in Saraya district, excluding 7 villages with a health post, will be eligible to participate. Saraya villages will be combined to form 24 clusters which will be randomized to receive HMM from a community volunteer, or IPTc plus HMM. Trained volunteer Community Medicine Distributors (CMD) will provide HMM. The primary endpoint will be the incidence of clinical malaria with fever or history of fever and parasitaemia with density of at least 3000/ul. Secondary outcomes will include the safety, the tolerability, the coverage and acceptability of the intervention. Both the recurrent and capital costs to the health service of training staff and delivering the interventions will be estimated. Both direct and indirect costs to users of the services (children and their families) will also be assessed.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Malaria
Keywords
IPTc, Community Case Management, Home Management for malaria

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
4554 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Community Case Management
Arm Type
Placebo Comparator
Arm Description
Provision of access to prompt diagnosis and treatment for malaria by community volunteers in the village (PECADOM)
Arm Title
Community Case Management plus IPTc
Arm Type
Experimental
Arm Description
Monthly Intermittent Preventive Treatment with sulfadoxine pyrimethamine plus amodiaquine, in addition to community case management
Intervention Type
Drug
Intervention Name(s)
IPTc+CCM
Intervention Description
Monthly administration of sulfadoxine-pyrimethamine plus amodiaquine, combined with community case management
Intervention Type
Drug
Intervention Name(s)
Community Case Management with artemether-lumefantrine (AL)
Intervention Description
Malaria diagnosis with Rapid Diagnostic Test and treatment with AL if the test is positive
Primary Outcome Measure Information:
Title
Number of children under 10 years of age with clinical malaria
Description
children under 10 years age presenting symptoms of malaria with fever (or history of fever in the previous 48 hours) with a positive Rapid Diagnostic Test or positive blood slides
Time Frame
up to 24 weeks
Secondary Outcome Measure Information:
Title
Number of children under 10 years of age presenting clinical Malaria with high parasite density
Description
Malaria with parasite density at 3000 parasites/uL or more in the presence of fever or history of fever in the previous 48hours in children under 10 years of age
Time Frame
up to 24 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
3 Months
Maximum Age & Unit of Time
10 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: age between 3 to 120 months consent participation given by parents or guardians willing to remain in the study area in the next 6 months Exclusion Criteria: Known allergy to the study investigational drug Any underlying chronic or severe condition. Participant under Treatment with sulfamides
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Oumar Gaye, PhD
Organizational Affiliation
Cheikh Anta Diop University, Senegal
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Paul Milligan, PhD
Organizational Affiliation
London School of Hygiene and Tropical Medicine
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Badara Cisse, PhD
Organizational Affiliation
Cheikh Anta Diop University, Senegal
Official's Role
Study Chair
Facility Information:
Facility Name
University Cheikh Anta Diop
City
Dakar
Country
Senegal

12. IPD Sharing Statement

Citations:
PubMed Identifier
30865632
Citation
Ndiaye JLA, Ndiaye Y, Ba MS, Faye B, Ndiaye M, Seck A, Tine R, Thior PM, Atwal S, Beshir K, Sutherland C, Gaye O, Milligan P. Seasonal malaria chemoprevention combined with community case management of malaria in children under 10 years of age, over 5 months, in south-east Senegal: A cluster-randomised trial. PLoS Med. 2019 Mar 13;16(3):e1002762. doi: 10.1371/journal.pmed.1002762. eCollection 2019 Mar.
Results Reference
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Trial of Malaria Seasonal IPTc Combined With Community Case Management

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