Alarcon 1989.
Methods | Randomized controlled trial Duration: dates not supplied. Participants followed up for 4 months |
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Participants | Number: 23 enrolled; numbers of males and females not presented Inclusion criteria: adults and children aged > 13 years, with 1 to 3 parenchymal cysts > 10 mm without perilesional oedema, good general health and stable neurological disease Exclusion criteria: parenchymal cysts with ring enhancement and oedema surrounding the lesions, pregnant women Type of lesion: viable |
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Interventions | Group 1. Albendazole: 15 mg/kg bodyweight for 3 days Group 2. Albendazole: 15 mg/kg bodyweight for 30 days Group 3. No albendazole | |
Outcomes | Included in the review: number of cysts and total diameter of cysts at baseline and 1 day, 30 days, and 3 months after treatment finishes. Adverse events | |
Notes | Location: Ecuador Source of funding: not stated |
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Risk of bias | ||
Bias | Authors' judgement | Support for judgement |
Adequate sequence generation? | Unclear risk | Quote: "randomly allocated" Decision: probably done, but unclear |
Allocation concealment? | Unclear risk | Not described |
Blinding? All outcomes | Unclear risk | Not described. Placebos were not used and different groups received follow‐up scans at different times Decision: unclear, probably not done |
Incomplete outcome data addressed? All outcomes | Low risk | 23 randomized and follow‐up data available for all (100%) |
Free of selective reporting? | Low risk | No evidence of selective reporting; outcomes reported individually for all participants |
Free of other bias? | Low risk | No evidence of other bias |