Repeat Ivermectin Mass Drug Administrations for MALaria Control II (RIMDAMAL II)
- Conditions
- Malaria
- Registration Number
- PACTR201907479787308
- Lead Sponsor
- Colorado State University
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- All
- Target Recruitment
- 4700
Residence in selected study village
Able to understand the information and willing to give consent or assent (age 12-18) and parent/guardian consent if study participant age is < 18 years of age.
Residence outside of the study village
Height < 90 cm (*note: if subject becomes =90cm over course the trial, this exclusion criteria will no longer be valid in subsequent MDA)
Current treatment with SP+AQ as part of SMC (restricted to children 3-48 months old) (*note: if subject discontinuous SP+AQ treatment because they become older than 48 months over course the trial, this exclusion criteria will no longer be valid in subsequent MDA)
Permanent disability or serious medical illness that prevents or impedes study participation and/or comprehension
Pregnancy (screened for in women of child-bearing age [ages 15-45] using a pregnancy urine rapid test [e.g. SD Bioline hCG] the week prior to each MDA)
Breast feeding if infant is within 1 week of birth Known allergy to ivermectin
Possibility of Loa loa infection as assessed by travel history to Angola, Cameroon, Chad, Central African Republic, Congo, Democratic Republic of Congo, Equatorial Guinea, Ethiopia, Gabon, Nigeria, and Sudan.
Enrolled in any other active clinical trials
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method