Anderson 1986.
| Methods | Randomization: no details Allocation concealment: no details Blinding: single (placebo and vaccine looked similar) Data collection: no details Intention to treat: yes Interim analysis: none Exclusion from analysis: none Follow‐up period: 8 days after vaccination |
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| Participants | Age: 8 to 60 months Health status: healthy Breastfeeding: 50 to 75% Immunization status: no information Clinical symptoms: clinical evaluation, no further details Laboratory studies: serology and stool analysis by ELISA |
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| Interventions | 1. Rhesus vaccine (MMU 18006), 10^6.5 PFU single dose (n = 13) 2. Placebo (similac formula), 30 ml single dose (n = 10) 30 ml similac formula given with vaccine or placebo |
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| Outcomes | 1. Safety: clinical symptoms within 8 days | |
| Notes | Study location: USA Two separate trials |
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