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Protocol Details

Natural History of Treated Neurocysticercosis and Long-Term Outcomes

This study is currently recruiting participants.

Summary | Eligibility | Citations | Contacts

Summary

Number

85-I-0127

Sponsoring Institute

National Institute of Allergy and Infectious Diseases (NIAID)

Recruitment Detail

Type: Participants currently recruited/enrolled
Gender: Male & Female
Min Age: 3 Years
Max Age: 99 Years

Referral Letter Required

No

Population Exclusion(s)

None

Keywords

Tapeworm;
Taenia Solium;
Neurocysticercosis;
Natural History;
Seizures;
Aseptic Meningitis;
Hydrocephalus

Recruitment Keyword(s)

None

Condition(s)

Cysticercosis;
Neurocysticercosis

Investigational Drug(s)

None

Investigational Device(s)

None

Intervention(s)

None

Supporting Site

National Institute of Allergy and Infectious Diseases

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 information, blood, urine samples, and additional cerebral spinal fluid if already being collected for clinical care.

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Eligibility

INCLUSION CRITERIA:

1. Patients ages 3 to 99 years.

2. Patients with proven or likely neurocysticercosis.

3. Willingness (of participant or legally authorized representative [LAR]) to sign consent and comply with study requirements.

EXCLUSION CRITERIA:

Not applicable.


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Citations:

Nash TE, Singh G, White AC, Rajshekhar V, Loeb JA, Proa(SqrRoot) o JV, Takayanagui OM, Gonzalez AE, Butman JA, DeGiorgio C, Del Brutto OH, Delgado-Escueta A, Evans CA, Gilman RH, Martinez SM, Medina MT, Pretell EJ, Teale J, Garcia HH. Treatment of neurocysticercosis: current status and future research needs. Neurology. 2006 Oct 10;67(7):1120-7.

Nash TE, Mahanty S, Garcia HH; Cysticercosis Group in Peru. Corticosteroid use in neurocysticercosis. Expert Rev Neurother. 2011 Aug;11(8):1175-83. doi: 10.1586/ern.11.86.

Nash TE, Garcia HH. Diagnosis and treatment of neurocysticercosis. Nat Rev Neurol. 2011 Sep 13;7(10):584-94. doi: 10.1038/nrneurol.2011.135. Review.

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Contacts:

Principal Investigator

Referral Contact

For more information:

Elise M. O'Connell, M.D.
National Institute of Allergy and Infectious Diseases (NIAID)
NIHBC 04 BG RM 424
4 MEMORIAL DR
BETHESDA MD 20892
(301) 761-5413
oconnellem@mail.nih.gov

Perla M. Adames Castillo, R.N.
National Institute of Allergy and Infectious Diseases (NIAID)
National Institutes of Health
Building 10
Room 6D44
10 Center Drive
Bethesda, Maryland 20892
(301) 402-8495
perla.adamescastillo@nih.gov

Office of Patient Recruitment
National Institutes of Health Clinical Center (CC)
Building 61, 10 Cloister Court
Bethesda, Maryland 20892
Toll Free: 1-800-411-1222
Local Phone: 301-451-4383
TTY: TTY Users Dial 7-1-1
ccopr@nih.gov

Clinical Trials Number:

NCT00001205

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