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Central Nervous System Disease in HIV-infected Children on HAART

Primary Purpose

HIV Infections, Central Nervous System Diseases

Status
Completed
Phase
Locations
United States
Study Type
Observational
Intervention
Sponsored by
National Cancer Institute (NCI)
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an observational trial for HIV Infections focused on measuring Encephalopathy, Neuroimaging, Cognition, Neuroinflammation, Opportunistic Infections, HIV, Central Nervous System Disease, Bipolar Disorder, Attention Deficit Hyperactivity Disorder, ADHD, Major Depression, Psychosis

Eligibility Criteria

undefined - undefined (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

-INCLUSION CRITERIA: HIV disease acquired in the first decade of life. Evidence of CNS disease (at least one of the following): Classification of encephalopathy or CNS compromise. Diagnosis of ADHD, bipolar disease, major depression, or psychosis For children greater than 7 years, ability to give assent if developmentally appropriate. EXCLUSION CRITERIA: Inability or unwillingness to provide informed consent for subjects greater than 18 years, and inability or unwillingness of one parent / legal guardian to provide consent for subjects less than 18 years. Clinically significant, unrelated systemic illness (serious infections or significant cardiac, pulmonary, hepatic or other organ dysfunction) which in the judgment of the Principal Investigator or Chairpersons would compromise the patient's ability to tolerate this study or is likely to interfere with the study procedures or results Lumbar Puncture Exclusion Criteria: Increased intracranial pressure (head imaging and neurologic examination to be performed prior to LP) Spinal cord lesion (to be screened by neurologic examination; spine imaging if clinically indicated) Platelet count less than 75,000/mm(3) Abnormal PT/PTT Focal suppuration at puncture site

Sites / Locations

  • National Institutes of Health Clinical Center, 9000 Rockville Pike

Outcomes

Primary Outcome Measures

Secondary Outcome Measures

Full Information

First Posted
May 5, 2005
Last Updated
December 11, 2019
Sponsor
National Cancer Institute (NCI)
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1. Study Identification

Unique Protocol Identification Number
NCT00110331
Brief Title
Central Nervous System Disease in HIV-infected Children on HAART
Study Type
Observational

2. Study Status

Record Verification Date
September 9, 2014
Overall Recruitment Status
Completed
Study Start Date
May 3, 2005 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
September 9, 2014 (undefined)

3. Sponsor/Collaborators

Name of the Sponsor
National Cancer Institute (NCI)

4. Oversight

5. Study Description

Brief Summary
This study will examine how HIV affects the brain and nervous system, learning, and behavior in children on highly active antiretroviral therapy (HAART). Although HAART has resulted in fewer HIV-infected children getting sick and even fewer dying from AIDS, many children on this treatment regimen develop significant brain or nervous system problems, such as learning difficulties, attention problems, hyperactivity, and depression. People who acquired HIV disease in the first decade of life and who have evidence of central nervous system (CNS) disease (e.g., encephalopathy, CNS compromise, ADHD, bipolar disease, major depression or psychosis) may be eligible for this study. Candidates are screened with a medical history, physical examination, neuropsychological testing and a CT scan of the head, if one has not been done within 12 months of entering the study. Participants undergo the following tests and procedures: MRI and MRS scan of the head: These tests use a magnetic field and radio waves to obtain images of the brain and detect changes in certain brain chemicals that may be affected by HIV infection. Both procedures are done at the same time. The patient lies on a table that is moved into the scanner (a narrow cylinder), wearing earplugs to muffle loud knocking and thumping sounds that occur during the scanning process. The procedure lasts about 50 to 60 minutes, during which time the patient can communicate with the staff. Neuropsychological testing: Patients' thinking and behavior are evaluated with tests to measure their memory, attention, language, problem-solving, academic, and motor skills and questionnaires to assess behavioral and emotional functioning, quality of life, and adherence to HIV medication. Parents are also asked to complete questionnaires assessing their child's behavioral and emotional functioning, quality of life, important life events, and adherence to HIV medication. Lumbar puncture (spinal tap): Cerebrospinal fluid (CSF) is collected for analysis. For this procedure, a local anesthetic is given and a needle is inserted in the space between the bones in the lower back where the CSF circulates below the spinal cord. Some fluid is collected through the needle. Blood tests and a physical examination are done before the procedure to make sure it can be done as safely as possible. Patients may also be sedated to prevent any discomfort. Follow-up: The blood tests, MRI and MRS scans and spinal tap are repeated 1 and 2 years after the initial evaluation. Some blood and spinal fluid samples from participants are stored for possible future studies related to HIV research
Detailed Description
Background: Highly active antiretroviral therapy (HAART) has altered the natural history of HIV disease in children. A significant minority of HIV-infected children has evidence of ongoing CNS disease. Specific markers for CNS disease, factors predictive of risk for neurological decline, and pathophysiologic mechanisms have not yet been identified in HIV-infected children. Objective: To explore the clinical features (neurological and psychiatric exams, neuropsychological evaluation, and neuroimaging), viral and neuroinflammatory factors, anatomic changes (brain MRI) and patterns of brain metabolites (1H-MRS) associated with HIV-related CNS disease in HIV-infected children in the HAART era. Eligibility: HIV disease acquired in the first decade of life. Evidence of CNS disease (classification of encephalopathy or CNS compromise or diagnosis of ADHD, bipolar disease, major depression, or psychosis). Design: Serial neurologic and psychiatric examinations, neuropsychologic test, neuroimaging, and CSF sampling will be performed once a year for a total of 3 evaluations.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
HIV Infections, Central Nervous System Diseases
Keywords
Encephalopathy, Neuroimaging, Cognition, Neuroinflammation, Opportunistic Infections, HIV, Central Nervous System Disease, Bipolar Disorder, Attention Deficit Hyperactivity Disorder, ADHD, Major Depression, Psychosis

7. Study Design

Enrollment
21 (Actual)

10. Eligibility

Sex
All
Accepts Healthy Volunteers
No
Eligibility Criteria
-INCLUSION CRITERIA: HIV disease acquired in the first decade of life. Evidence of CNS disease (at least one of the following): Classification of encephalopathy or CNS compromise. Diagnosis of ADHD, bipolar disease, major depression, or psychosis For children greater than 7 years, ability to give assent if developmentally appropriate. EXCLUSION CRITERIA: Inability or unwillingness to provide informed consent for subjects greater than 18 years, and inability or unwillingness of one parent / legal guardian to provide consent for subjects less than 18 years. Clinically significant, unrelated systemic illness (serious infections or significant cardiac, pulmonary, hepatic or other organ dysfunction) which in the judgment of the Principal Investigator or Chairpersons would compromise the patient's ability to tolerate this study or is likely to interfere with the study procedures or results Lumbar Puncture Exclusion Criteria: Increased intracranial pressure (head imaging and neurologic examination to be performed prior to LP) Spinal cord lesion (to be screened by neurologic examination; spine imaging if clinically indicated) Platelet count less than 75,000/mm(3) Abnormal PT/PTT Focal suppuration at puncture site
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Rohan Hazra, M.D.
Organizational Affiliation
National Cancer Institute (NCI)
Official's Role
Principal Investigator
Facility Information:
Facility Name
National Institutes of Health Clinical Center, 9000 Rockville Pike
City
Bethesda
State/Province
Maryland
ZIP/Postal Code
20892
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
11794218
Citation
Gortmaker SL, Hughes M, Cervia J, Brady M, Johnson GM, Seage GR 3rd, Song LY, Dankner WM, Oleske JM; Pediatric AIDS Clinical Trials Group Protocol 219 Team. Effect of combination therapy including protease inhibitors on mortality among children and adolescents infected with HIV-1. N Engl J Med. 2001 Nov 22;345(21):1522-8. doi: 10.1056/NEJMoa011157.
Results Reference
background
PubMed Identifier
3000281
Citation
Belman AL, Ultmann MH, Horoupian D, Novick B, Spiro AJ, Rubinstein A, Kurtzberg D, Cone-Wesson B. Neurological complications in infants and children with acquired immune deficiency syndrome. Ann Neurol. 1985 Nov;18(5):560-6. doi: 10.1002/ana.410180509.
Results Reference
background
PubMed Identifier
12949303
Citation
Tamula MA, Wolters PL, Walsek C, Zeichner S, Civitello L. Cognitive decline with immunologic and virologic stability in four children with human immunodeficiency virus disease. Pediatrics. 2003 Sep;112(3 Pt 1):679-84. doi: 10.1542/peds.112.3.679.
Results Reference
background

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Central Nervous System Disease in HIV-infected Children on HAART

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