Skip to main content
OpenTrials
Completed

NCT Number: NCT00782808

Peripheral Reservoir of HIV DNA in Monocytes Pivotal to Cognition in HIV

Sixty HIV participants will be enrolled and stratified by PBMC HIV DNA levels, either high (greater than or equal to 5000 copies/106 cells) or low (less than 5000 copies/106 cells). Individuals will be enrolled into each group until filled. Screening PBMC HIV DNA levels will be performed at SEARCH in real-time with less than one-week turn around time. All individuals will intend to initiate ARV due to meeting MOPH guidelines for such. The protocol team will work with the primary care physician to facilitate initiation of standard ARV care; however, initiation of ARV is not a requirement of the study and ARV will not be provided by the study.

Completed

Looking for future studies?

Notify Me

Key information

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • HIV-infected individuals meeting MOPH criteria to initiate HAART and planning to initiate HAART within a month of screening.
  • Consequently, all participants will have plasma CD4 counts at less than 250 cells.

Exclusion criteria

  • Head injury with loss of consciousness greater than 1 hour or cognitive sequela
  • Current/past illicit drug use or positive drug screen for methamphetamines, amphetamines, or cocaine at screening or entry.
  • Any of the following laboratory abnormalities:
  • PT/PTT > the upper limit of normal (ULN) or INR > 1.1
  • Hemoglobin < 9.0 mg/dL
  • ALT > 5x ULN
  • serum creatinine > 2x ULN or creatinine clearance < 30 cc per min by Cockroft-Gault formula
  • Acute illness within 30 days prior, persistent and active AIDS-defining OI of any organ system or autoimmune disease.
  • Current or recent fevers or meningeal signs suggestive of CNS opportunistic infection
  • CNS opportunistic infection, past or present (Patients diagnosed with opportunistic infection after CSF examination will be excluded from further analysis. In such a situation, an additional patient will be enrolled)
  • History of pre-existing neurologic disease to include stroke, multiple sclerosis or psychiatric illness including schizophrenia, bipolar disorder, anxiety disorder, panic attacks, major depression, or post traumatic stress disorder. Patients with past depression that is controlled and patients with or minor depressive symptoms will be allowed to enroll.
  • Known learning disability including dyslexia or unable to read or write basic Thai
  • Positive Hepatitis C serology (Hepatitis C Ab)
  • Confusion or other signs and symptoms of metabolic encephalopathy or delirium
  • Other conditions that could explain neurocognitive decline in the opinion of the investigator such as hypothyroidism, vitamin B12 deficiency or neurosyphilis
  • Pregnancy or metal objects that would preclude MRI

Treatment and study plan

Primary outcomes

  1. To determine the long-term relationship between cognition and HIV DNA in circulating PBMCs and monocytes (CD14+ PBMCs) among patients initiating HAART for the first time

    Time frame: After March 30, 2016

Sponsors and collaborators

Lead sponsor

SEARCH Research Foundation

Other

Collaborators

  • National Institute of Neurological Disorders and Stroke (NINDS)

Registry information

Important dates

Study start
2009
Primary completion
2014
Study completion
2014
First posted
Oct 31, 2008
Registry last updated
Sep 26, 2014

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.