Skip to main content
. 2005 Apr 20;2005(2):CD004614. doi: 10.1002/14651858.CD004614.pub2

Ansah 2003.

Methods Quasi‐randomized controlled trial
Generation of allocation sequence: alternate allocation
Allocation concealment: no information provided
Blinding of outcome assessor: none
Completeness of outcome data: 99%
Participants Participants: 299 analysed (155 intervention; 144 control); 301 initially recruited
Inclusion criteria: aged 0 to 5 years; brought to 1 of 2 clinics with malaria
Exclusion criteria: none given, but 2 participants excluded on developing severe malaria
Mean age: not stated
Age range: not stated
Male to female ratio: not stated
Education: not stated
Interventions See Appendix 2 for details
Outcomes
  1. Treatment adherence: number of participants following the prescribers' exact instructions in terms of dosage (spoon size for syrup not taken into account), frequency of daily administration, and duration of treatment; measured by participant interview

  2. Caregivers' assessment of wellness at day 4

  3. Vomiting of tablets


Not included in review:
  1. Packaging acceptability and preference

  2. Financial and economic costs

Notes Location: Cape Coast, Ghana
Health facilities: 2 public health centres
Endemicity: highly endemic malaria
Antimalarial drug resistance: not stated
Malaria diagnosis: clinical (Plasmodium falciparum causes most morbidity and mortality in this area)