A Pilot Study of Neurocysticercosis Treatment
Neurocysticercosis
About this trial
This is an interventional treatment trial for Neurocysticercosis focused on measuring neurocysticercosis, albendazole, tape worm
Eligibility Criteria
Inclusion Criteria: Patients presenting with new onset of symptoms associated with neurocysticercosis within two months of identification and have active and/or transitional neurocysticercosis cysts on computed tomography (CT) or magnetic resonance imaging (MRI) Exclusion Criteria: Patients with only calcifications Patients who are pregnant Patients with one of the following conditions: papilledema, active tuberculosis, syphilis, ocular cysticercosis, active gastric ulcers, or a progressive and life-threatening disorder Patients who received anthelmintic drugs (AHD) during the year preceding presentation or who received steroids within 30 days of presentation
Sites / Locations
- Vicente Corral Moscoso Hospital of Cuenca, Centro de Epilepsia, Facultad de Ciencias Médicinas de la Universidad de Cuenca IDIUC (Área 5), Av. 12 de Abril. Cdla.
- Teodoro Maldonado Carbo Hospital, Av. 25 de Julio Vía Puerto Marítimo
- Baca Ortiz Children's Hospital, Av. Colon s/n y 6 de Diciembre
- Hospital Carlos Andrade Marin, Av. 10 de agosto y Bogotá
- Hospital Eugenio Espejo, Servicio de Neurología, Av. Colombia s/n
Arms of the Study
Arm 1
Arm 2
Active Comparator
Placebo Comparator
1
2
albendazole, 15 mg/kg/day for those less than 50 kg in weight. For those more than 50 kg, 800 mg was administered. All got standard symptomatic therapy placebo plus standard symptomatic therapy