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NCT Number: NCT00187512

SCOPE: Observational Study of the Consequences of the Protease Inhibitor Era

SCOPE is an observational, prospective study of HIV-1 infected volunteers designed to provide a specimen bank of samples with carefully characterized clinical data. SCOPE specimens will be used to examine multiple questions involving virologic, immunologic, and host factors involved in HIV-1 infection, progression, non-progression, response to treatment, control of HIV-1 virus, and evolution of drug resistance.

Recruiting

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

About this study

SCOPE is an observational, prospective study of HIV-1 infected volunteers designed to provide a specimen bank of samples with carefully characterized clinical data. Samples from SCOPE will be used to examine:

  • Virologic, immunologic, and host factors involved in the natural control of HIV-1 infection (long term non-progression and/or virologic control of HIV-1 without antiretroviral therapy)
  • Virologic and immune correlates associated with disease progression
  • Evolution of antiretroviral drug resistance
  • Factors associated with transmission or acquisition of HIV infection

Enrolled subjects are seen at San Francisco General Hospital every four months for a detailed interview, saliva collection, and blood draw. Baseline visits take approximately one hour, follow up visits take approximately 20-40 minutes. No personal identifiers are used for specimen bank samples.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

SCOPE is currently recruiting HIV-1 infected subjects with any of the following criteria:

  • Documented HIV viral load less than 2000 copies/ml WITHOUT taking antiretroviral therapy
  • Undetectable HIV viral load with CD4 T-cells consistently less than 350 for the last 12 months while taking a stable antiretroviral regimen.
  • Antiretroviral naive and planning to start an antiretroviral regimen - any CD4 or HIV viral load acceptable.
  • Long-term Non Progressors: HIV-positive at least 10 years, no antiretroviral therapy for the past 10 years or more, any viral load acceptable, CD4-T cell count always above 500.

Exclusion criteria

  • Active opportunistic infection or systemic treatment for opportunistic infection within the last 4 months (oral candidiasis acceptable)
  • Active treatment for cancer
  • Active treatment for hepatitis C requiring interferon based therapy
  • Immunosuppressive therapy taken within the last 4 months

Treatment and study plan

Primary outcomes

  1. The general theme of this core is to investigate the relationship between the virologic response to antiretroviral therapy and clinical outcome.

    Time frame: Ongoing

Study contacts

Contact information is provided by the study sponsor or research team.

Montha Pao

CONTACT

[email protected]

415-476-4082 ext. 140

Rebecca Hoh, M.S., R.D.

CONTACT

[email protected]

415-476-4082 ext. 139

Sponsors and collaborators

Lead sponsor

University of California, San Francisco

Other

Collaborators

  • National Institute of Allergy and Infectious Diseases (NIAID)

Registry information

Acronym: SCOPE

Important dates

Study start
2000
Primary completion
2032
Study completion
2033
First posted
Sep 16, 2005
Registry last updated
Jul 8, 2025

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.

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