Natural History of Treated Neurocysticercosis and Long-Term Outcomes

Part of paid clinical trials in Bethesda, Maryland.

Sponsor
National Institute of Allergy and Infectious Diseases (NIAID)
Study ID
NCT00001205
Status
Recruiting

Conditions

  • Cysticercosis
  • Neurocysticercosis

Eligibility Criteria

Sex
ALL
Age
3 Years - 99 Years
Healthy Volunteers
Accepted

Study Details

Neurocysticercosis is a brain disease due to the larval stage of the pork tapeworm (Taenia solium). The most common symptoms patient experience from infection inside the substance of the brain (parenchymal disease) are seizures and headaches. When the infection is either inside the fluid pockets inside the brain (ventricular disease) or in the space around the brain (subarachnoid disease) patients can have chronic headaches, relapsing aseptic meningitis, hydrocephalus, stroke, and may require neurosurgical intervention. The purpose of this study is to treat patients with anthelmintic therapy (praziquantel and/or albendazole) and anti-inflammatories in alignment with currently accepted best practices and guidelines, depending on the neurocysticercosis subtype. The purpose of the study is to better understand and characterize clinical, biologic, and management factors during treatment that influence long term outcomes. In order to understand this further we collect patient clinical information, patient survey responses, blood, urine samples, and additional cerebral spinal fluid if already being collected for clinical care....

Key Dates

Start date
Oct 7, 1985
Status verified
Mar 2026

Study Design

Enrollment
500 participants (estimated)

Arms

  • Arm: Arm 1
    Subarachnoid (racemose) neurocysticercosis
  • Arm: Arm 2
    Ventricular without other viable disease
  • Arm: Arm 3
    Parenchymal cyst(s)--non-calcified parenchymal disease at time of referral
  • Arm: Arm 4
    Calcified parenchymal disease with symptoms (seizures)
  • Arm: Arm 5
    Calcified parenchymal disease without symptoms
  • Arm: Arm 6
    Endemic exposure--subjects with compatible epidemiologic exposure to T. solium

Primary Outcome Measure

The primary objective is to characterize the biochemical and clinical course of neurocysticercosis (NCC) during and after treatment with long-term follow-up. [ Time Frame: Ongoing ]

Central Contacts

Locations (1)

FacilityCityStateZIPSite coordinators
National Institutes of Health Clinical CenterBethesdaMaryland20892-

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