Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-25 @ 4:18 AM
Ignite Modification Date:
2025-12-25 @ 4:18 AM
NCT ID:
NCT01694420
Eligibility Criteria:
Acute HIV infection is defined as:
1. A positive 4th generation HIV Ag/Ab Combination Assay and HIV RNA (NAAT or viral load) and one of the following within 30 days of study entry:
* a negative HIV rapid test
* negative/indeterminate Western Blot
OR
2. A negative or indeterminate HIV antibody, antigen, or nucleic acid amplification test (NAAT) and any one of the following within 30 days of study entry:
* A detectable HIV nucleic acid in blood confirmed by a second NAAT
* Positive p24 antigen
* A positive HIV antibody test according to standard criteria obtained within 45 days after an initial negative or indeterminate HIV antibody, antigen, or nucleic acid amplification.
Inclusion Criteria:
1. Acute HIV Infection (as defined above) within 30 days of study entry.
2. Age \>18 years.
3. ART-naive (\<14 days of previous antiretroviral treatment. Exceptions are: Post-exposure prophylaxis (PEP) if participant was documented as HIV-negative at least 3 months after completion of PEP.
4. Lab values within 30 days prior to study entry:
1. Absolute neutrophil count \>500/mm3
2. Hemoglobin \> 8.5 g/dL for men and \> 8.0 g/dL for women
3. Platelet count \>50,000/mm3
4. AST (SGOT)\> .2.5 x ULN
5. ALT (SGPT)\> .2.5 x ULN
6. Total bilirubin \<2.5 x ULN
7. Calculated creatinine clearance (Cockcroft-Gault formula) \> 70mL/min:
5. For women of reproductive potential, a negative pregnancy test within 72 hours prior to initiating antiretroviral study medications. Reproductive potential is defined as females who have reached menarche and have not been post-menopausal for at least 24 consecutive months, or have not undergone surgical sterilization.
6. Female study participants must use a reliable form of barrier contraception, such as a condom, even if they also use other methods of birth control. All participants must continue to use contraception for 12 weeks after stopping study medications. Acceptable methods of barrier contraception include: condoms (male or female), diaphragm, or cervical cap. These can be used alone or in tandem with hormonal or IUD method.
7. Ability and willingness of participant to give written informed consent.
Exclusion Criteria:
1. Women who are pregnant or breast-feeding.
2. Women with a positive pregnancy test prior to study drug administration.
3. Men who have sex with women, and women of reproductive potential unwilling or unable to use an acceptable, reliable barrier method of contraception for the entire study period and 12 weeks afterwards.
4. Use of immunomodulators (e.g., interleukins, interferons, cyclosporine), HIV vaccine, systemic cytotoxic chemotherapy, or investigational therapy within 30 days of study entry (Prednisone 10 mg QD or less is permitted.
5. Known allergy/sensitivity to study drugs
6. Difficulty swallowing pills
7. Inability to communicate effectively with study personnel
8. Incarceration; prisoner recruitment and participation are not permitted
9. Active drug or alcohol use that, in the opinion of the site investigator, would interfere with participation in the study
10. Any active psychiatric illness that, in the opinion of the investigator, could confound the analysis of the neurological examination or neuropsychological test results
11. Active brain infection (except for HIV-1), brain neoplasm, space-occupying brain lesion requiring acute or chronic therapy
12. Serious illness requiring systemic treatment and/or hospitalization until patient either completes therapy or is clinically stable on therapy for at least 7 days prior to study entry
13. Known cardiac conduction disease
14. Prior treatment with any other experimental drug within 30 days of initiating study treatment
15. Unable to discontinue any current medications that are excluded during study treatment
16. Life expectancy less than twelve months
17. Acute Viral Hepatitis, including, but not limited to, Hepatitis A, B, or C
18. Chronic Hepatitis B Infection documented by a detectable serum Hepatitis B surface antigen (HBsAg) or plasma HBV DNA
19. Calculated creatinine clearance (Cockcroft-Gault formula) \<70mL/min
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Maximum Age:
75 Years
Study:
NCT01694420
Study Brief:
Protocol Section:
NCT01694420