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Clinical Trial Details — Status: Withdrawn

Administrative data

NCT number NCT03308331
Other study ID # HP-00075780
Secondary ID
Status Withdrawn
Phase N/A
First received
Last updated
Start date December 1, 2019
Est. completion date October 30, 2025

Study information

Verified date March 2020
Source University of Maryland, Baltimore
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

People living with HIV-1 have high rates of cigarette smoking, which may be related to nicotinic interaction with HIV-1 infection and brain function levels. The proposed project aims to understand these pathways using translational brain imaging and HIV-1 reactivation studies. The study proposes a targeted nicotine-brain investigation of the nicotinic effects in HIV-1 infection from cellular to brain circuitry levels.


Description:

Smoking remains the leading cause of preventable morbidity and mortality in the United States. The alarmingly high smoking rates and unsatisfactory performance of standard smoking cessation efforts in people living with HIV/AIDS (PLWH) interfere with the overall progress in the treatment of HIV-1 infection. Our understanding of nicotine addiction mechanisms in PLWH, and how they are related to and interact with HIV-1 neuropathology, is limited and thus hindering the development of more effective, targeted treatments. The study will directly address neurological complication of this HIV-associated comorbidity at the brain circuitry level using state-of-the-art imaging tools and methods.


Recruitment information / eligibility

Status Withdrawn
Enrollment 0
Est. completion date October 30, 2025
Est. primary completion date October 30, 2025
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 60 Years
Eligibility Inclusion Criteria:

1. Subjects between ages 18-60 in good health

2. Ability to give written informed consent

3. For people living with HIV: should be diagnosed with HIV two years or more and on ART two years or more

4. For people living with HIV: should have achieved virologic suppression (defined as viral loads of = 200 copies/ml), and without current signs of reactivation

Exclusion Criteria:

1. Inability to sign informed consent

2. Unable to undergo MRI scanning due to metallic devices or objects (cardiac pacemaker or neurostimulator, some artificial joints, metal pins, surgical clips or other implanted metal parts) or claustrophobic to the scanner

3. Any major medical illnesses to include, but not limited to, uncontrolled high blood pressure or high blood sugar, cardiovascular disease, asthma, peripheral vascular diseases, coagulopathies, history of superficial or deep vein thrombosis as per medical history

4. Current substance-induced psychiatric disorders

5. Significant alcohol or other drug use, other than nicotine dependence or marijuana use

6. Gross structural abnormalities and/or have a history of syncope

7. Positive urine pregnancy tests

8. Any neurological illnesses to include, but not limited to, seizure disorders, multiple sclerosis, movement disorders, or history of head trauma, CVA, CNS tumor,

9. For people living with HIV: having AIDS or non-AIDS-defining cancer or active CNS and other opportunistic disease

10. For people living with HIV: on active treatment of hepatitis C virus (HCV)

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Tobacco smoking and nicotine patch
Tobacco smoking at each participant's regular cigarette. Over-the-counter nicotine patch use

Locations

Country Name City State
United States University of Maryland School of Medicine Baltimore Maryland

Sponsors (1)

Lead Sponsor Collaborator
University of Maryland, Baltimore

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Functional and structural connectivity using magnetic resonance imaging (MRI) Resting functional MRI and diffusion imaging MRI one day
Secondary HIV-1 reactivation HIV-1 viral protein p24 expression one day
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