Anthelmintic Treatment for Neurocysticercosis

Natural History of Treated Neurocysticercosis and Long-Term Outcomes

Recruiting Observational Study
Cysticercosis Neurocysticercosis
No Placebo Group Every participant receives an active treatment — no one gets a placebo. Healthy Volunteers Welcome You do not need to have the condition being studied to take part. No Study Drug Researchers observe your health over time — no experimental treatment is given.
Ready to participate?

Review the details below, then apply to join this clinical trial.

At a Glance
Age
3 – 99
Sex
Any
Study type
Observational
Participants needed
500 (estimated)
Sponsor
National Institute of Allergy and Infectious Diseases (NIAID) · NIH
Who this trial is looking for

This trial is looking for patients aged 3 and older who have neurocysticercosis or are likely to have it. Participants will receive treatment and their clinical information will be collected to understand long-term outcomes better.

Are You a Good Fit for This Trial?

You may be able to join if

  • I am aged 3 years or older.
  • I can understand and sign a consent form.
  • I have been diagnosed with neurocysticercosis or it is likely.

Summarized in plain language from this trial's official eligibility criteria. The full criteria are further down this page — only the research team can confirm whether you qualify.

Think this trial could be right for you?

Answer a few quick questions to see if you may meet the eligibility requirements.

Check Your Eligibility
About This Trial
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…
Trial Locations
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Eligibility Criteria
* INCLUSION CRITERIA: Arms 1-5 (NCC): 1. Aged 3 years and older. 2. Ability of participant (or legally authorized representative, LAR) to understand and the willingness to sign a written informed consent document. 3. Patients with proven or likely NCC Arm 6 (Endemic Exposures): 1. Patient with e…
Contacts

Perla M Adames Castillo, R.N.

(301) 402-8495

perla.adamescastillo@nih.gov

CONTACT

Elise M O'Connell, M.D.

(301) 761-5413

oconnellem@mail.nih.gov

CONTACT