- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT00260936
Metabolic Abnormalities - HIV Infected and Uninfected Males
27. februar 2017 opdateret af: University of North Carolina, Chapel Hill
Prevalence of Morphologic and Metabolic Anormalities in HIV Infected and Uninfected Young Men
To assess whether there exist significant differences in glucose metabolism, lipids, lactate, body composition, and bone density between HIV-infected and uninfected young men.
Studieoversigt
Status
Afsluttet
Betingelser
Detaljeret beskrivelse
The study involves a one-time collection of health and medical history data, blood and urine specimens, and physical assessments.
This study will elucidate the need for a further in-depth study to understand the pathophysiological effects of protease inhibitor (PI)-based and non-nucleoside analogue reverse transcriptase inhibitor (NNRTI)-based therapies in young men.
Undersøgelsestype
Observationel
Tilmelding (Faktiske)
250
Kontakter og lokationer
Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.
Studiesteder
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California
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Los Angeles, California, Forenede Stater, 90054
- Childrens Hospital of Los Angeles
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San Diego, California, Forenede Stater, 92093
- University of California at San Diego
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San Francisco, California, Forenede Stater, 94143
- University of California at San Francisco
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District of Columbia
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Washington, District of Columbia, Forenede Stater, 20010
- Childrens Hopital National Medical Center
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Florida
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Fort Lauderdale, Florida, Forenede Stater, 33301
- Children's Diagnoistic and Treatment Center
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Miami, Florida, Forenede Stater, 33101
- University of Miami
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Tampa, Florida, Forenede Stater, 33606
- University of South Florida
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Illinois
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Chicago, Illinois, Forenede Stater, 60612
- Stroger Hospital of Cook County
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Massachusetts
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Boston, Massachusetts, Forenede Stater, 02115
- Children's Hopsital of Boston
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New York
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Bronx, New York, Forenede Stater, 10467
- Montefiore Medical Center
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New York, New York, Forenede Stater, 10128
- Mount Siani Medical Center
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Pennsylvania
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Philadelphia, Pennsylvania, Forenede Stater, 02115
- Children's Hospital of Philadelphia
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San Juan, Puerto Rico, 00936
- University Pediatric Hospital
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Deltagelseskriterier
Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.
Berettigelseskriterier
Aldre berettiget til at studere
12 år til 24 år (Barn, Voksen)
Tager imod sunde frivillige
Ja
Køn, der er berettiget til at studere
Han
Prøveudtagningsmetode
Ikke-sandsynlighedsprøve
Studiebefolkning
Approximately 250 subjects will be enrolled in the study.
The number of subjects enrolled in each study group will be as follows: 50 HIV-negative subjects; 100 HIV-positive subjects who are antiretroviral therapy (ART) naïve; and two groups of up to 50 HIV-positive subjects each, one on an NNRTI-based regimen and the other on a PI-based regimen.
Beskrivelse
Inclusion Criteria:
- Males age 12 years and 0 days through 24 years and 364 days.
- Tanner stage 4 or 5.
- Accessible medical history and medications history.
- Willingness to fast and complete all clinical evaluations and specimen collection.
- Willingness and ability to give informed consent or assent with parental/legal guardian permission, where required.
Group 1: HIV-Negative Control Subject Specific Inclusion Criteria
- All subjects for Group 1 will be tested for HIV-1 to confirm negativity unless they have a documented negative antibody test within the last three months of study entry.
- Willingness and ability to give informed consent for HIV testing. Groups 2, 3, and 4: HIV-Positive Subject Specific Inclusion Criteria
- HIV-1 infection as documented by a positive result on any of the following licensed tests at any time: any antibody test confirmed by Western blot, HIV culture, plasma HIV-1 RNA PCR >1,000 copies/ml or HIV-1 DNA PCR.
- Horizontal HIV infection transmission (non-perinatal, non-transfusion acquired infection).
- Group 2: Currently not on ART and must never have received ART.
- Group 3: Currently on a NNRTI, non-PI containing regimen for three or more months, must never have received a total of more than six months of PI-containing regimen and at least one year must have passed since receipt of last PI-containing regimen.
- Group 4: Currently on a PI, non-NNRTI containing regimen for three or more months, must never have received a total of more than six months of NNRTI-containing regimen and at least one year must have passed since receipt of last NNRTI-containing regimen.
Exclusion Criteria:
- Transgender male to female (MTF) or female to male (FTM) youth
- Refusal to fast for the 8 hours before collection of laboratory specimen requiring fasting.
- Unable to obtain medical/medications history.
- History of anorexia or bulimia.
- Type I Diabetes Mellitus.
- Type II Diabetes Mellitus and cannot omit diabetes medication for the 48-hour period prior to laboratory specimen collection for oral glucose tolerance test (OGTT).
- Current use or use within the past 6 months of oxandrolone, nandrolone, oxymetholone, stanozolol, or any other synthetic anabolic/androgenic agents.
- Current use or use within the past 6 months of pharmacologic doses of growth hormone. Physiologic growth hormone replacement therapy is permitted, as long as dosages meet the following specifications:
- Adolescents in puberty - less than or equal to an equivalent of 0.1 mg/kg/day
- Adolescents past puberty - less than or equal to an equivalent of 0.025 mg/kg/day
- Current use or use within the past 6 months of pharmacologic doses of testosterone. Physiologic testosterone replacement therapy is permitted as long as dosages meet the following specifications:
- Injection - no more than 400 mg/month of testosterone enanthate
- Patch - no more than 5 mg/day (e.g. Testoderm, Androderm)
- Gel in pre-packaged doses - no more than 7.5 g/day of gel (e.g. Androgel, Testim)
Studieplan
Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
Kohorter og interventioner
Gruppe / kohorte |
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HIV-negative
HIV-infected and -uninfected males, ages 12 to 24 years, of Tanner Stage 4 or 5
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HIV-positive, has never been on ART
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HIV-positive, non PI containing NNRTI-based regimen
HIV-positive, currently on a non-PI-containing NNRTI-based regimen for at least 12 weeks.
Must never have received a total of more than 6 months of PI-containing regimen, and at least one year must have passed since receipt of last PI-containing regimen
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HIV-positive, non-NNRTI-containing PI-based regimen
HIV-positive, currently on a non-NNRTI-containing PI-based regimen for at least 12 weeks.
Must never have received a total of more than 6 months of NNRTI-containing regimen, and at least one year must have passed since receipt of last NNRTI-containing regimen.
|
Samarbejdspartnere og efterforskere
Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.
Efterforskere
- Studiestol: Grace Aldrovandi, MD, Children's Hospital Los Angeles
Publikationer og nyttige links
Den person, der er ansvarlig for at indtaste oplysninger om undersøgelsen, leverer frivilligt disse publikationer. Disse kan handle om alt relateret til undersøgelsen.
Hjælpsomme links
Datoer for undersøgelser
Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.
Studer store datoer
Studiestart
1. marts 2006
Primær færdiggørelse (Faktiske)
1. august 2007
Studieafslutning (Faktiske)
1. august 2007
Datoer for studieregistrering
Først indsendt
30. november 2005
Først indsendt, der opfyldte QC-kriterier
30. november 2005
Først opslået (Skøn)
2. december 2005
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
1. marts 2017
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
27. februar 2017
Sidst verificeret
1. februar 2016
Mere information
Begreber relateret til denne undersøgelse
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
- ATN 021b
Disse oplysninger blev hentet direkte fra webstedet clinicaltrials.gov uden ændringer. Hvis du har nogen anmodninger om at ændre, fjerne eller opdatere dine undersøgelsesoplysninger, bedes du kontakte register@clinicaltrials.gov. Så snart en ændring er implementeret på clinicaltrials.gov, vil denne også blive opdateret automatisk på vores hjemmeside .