Amoebiasis Infections and Infestations Amoebiasis
Conditions
Interventions
To determine the sample size, we used a <0.05 and power of study as 90%. The effect size considered to be clinically significant, was a 0.15 difference between two groups based on a pilot study. ?Hypo
Sponsors
Hamdard University (Pakistan)
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1. All the confirmed cases of amoebiasis and between the ages of 5 and 60 years were invited to be included in the study 2. Willing to be assigned to any of the two treatment groups
Exclusion criteria
Exclusion criteria: All those who had multiple problems
Design outcomes
Secondary
| Measure | Time frame |
|---|---|
| 1. Side effects 2. Association of age with efficacy 3. Association of sex with efficacy 4. Association of age with side effects 5. Association of sex with side effects Measured at baseline and immediately after completion of course of treatment. | — |
Primary
| Measure | Time frame |
|---|---|
| Efficacy at baseline and 5 days after stopping the treatment | — |
Countries
Pakistan
Outcome results
None listed