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Manhattan HIV/Hepatology Brain Bank

Manhattan HIV/Hepatology Brain Bank

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT00300209
Enrollment
187
Registered
2006-03-08
Start date
1998-09-30
Completion date
2002-06-30
Last updated
2016-03-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hepatitis, HIV

Brief summary

Description: The Manhattan HIV/Hepatology Brain Bank (MHBB) was established in 1998 as a resource for the AIDS research community. The MHBB was created to act as a center for the provision of pre- and post-mortem tissues and body fluids from HIV infected persons. It has recently expanded its goals to assist in the elucidation of liver disease-induced nervous system disorders. The MHBB is dedicated to improving the understanding of HIV and Hepatitis C and thereby, improving the lives of patients living with HIV and/or Hepatitis C. Participation is voluntary and can be stopped at any time. Benefits: This is an observational study; no experimental procedures, devices or drugs are used. All enrolled patients undergo regular examinations by physicians, nurses, and neuropsychologists who specialize in the problems that HIV and HCV can cause. Taking part in this study may result in the detection of brain, muscle, or spinal cord disease for which treatments may be available. Participants may receive no direct benefit from this study. However, knowledge gained from this research may, in the future, help others who suffer from HIV/AIDS and/or liver disease. Participants agree to autopsy and organ donation upon demise by signing an Anatomical Gift Consent document.

Interventions

None listed

Sponsors

National Institute of Mental Health (NIMH)
CollaboratorNIH
Icahn School of Medicine at Mount Sinai
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

CD4 \< 50 on two occasions \>12 weeks apart. Hemoglobin \<10 G/dL. Albumin \<3.2 G/dL. CMV end-organ disease Disseminated MAC PML AIDS Dementia Complex Wasting (\>30% of lean body mass) Visceral Kaposi's sarcoma Lymphoma-systemic of CNS CHF Major systemic illness with poor prognosis (as determined by primary physician).

Exclusion criteria

\- \<18 years old Not willing to sign an Anatomical Gift Consent for autopsy and organ donation upon demise.

Design outcomes

Primary

MeasureTime frameDescription
Viral Load blood levelBaselinePlasma viral load level

Secondary

MeasureTime frame
CD4 cell blood levelBaseline

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026