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 1Subarachnoid (racemose) neurocysticercosis
- Arm: Arm 2Ventricular without other viable disease
- Arm: Arm 3Parenchymal cyst(s)--non-calcified parenchymal disease at time of referral
- Arm: Arm 4Calcified parenchymal disease with symptoms (seizures)
- Arm: Arm 5Calcified parenchymal disease without symptoms
- Arm: Arm 6Endemic 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
- Perla M Adames Castillo, R.N.(301) 402-8495
- Elise M O'Connell, M.D.(301) 761-5413
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| National Institutes of Health Clinical Center | Bethesda | Maryland | 20892 | - |