An Open-Label, Randomized, Three-Arm, Comparative Trial of a Caloric Supplement With Peptides and Medium-Chain Triglycerides Versus a Caloric Supplement With Whole Protein and Long-Chain Triglycerides Versus No Caloric Supplement for the Prevention of Weight Loss in Individuals With AIDS Who Take a Daily Multivitamin and Mineral Supplement
Complément alimentaire Data
+ dietarySupplement Data
+ dietarySupplement Data
Données recueillies dès le début de l'étude - ProspectiveInfections transmises par le sang+23
+ Maladies génito-urinaires
+ Maladies Génitales
Cohorte
Suivi d'un groupe de personnes dans le temps pour mieux comprendre les causes et l'évolution d'une maladie.Résumé
Date de début de l'étude : 1 juin 1996
Date à laquelle le premier participant a commencé l'étude.Patients will be randomized to one of 3 study arms: Arm 1 - Peptamen drinks + multivitamin and mineral supplement, taken in addition to regular diet for 4 months Arm 2 - NuBasics drinks or equivalent amounts of NuBasics soups or bars + multivitamin and mineral supplement, taken in addition to regular diet for 4 months Arm 3 - Multivitamin and mineral supplement, taken in addition to regular diet for 4 months. At months 0, 2, and 4, patients will be assessed for weight, body cell mass, patient-reported physical activity level, and dietary intake (by 24-hour dietary recall). At months 2 and 4, they will also be assessed for compliance with study regimen. Patients who complete their 4 month follow up visit will be provided with a 30 day supply of the caloric supplement of their choice (Peptamen or NuBasics) and a 30 day supply of the study multivitamin supplement.
Protocole
Cette section fournit des détails sur le plan de l'étude, y compris la manière dont l'étude est conçue et ce qu'elle évalue.536 participants à inclure
Nombre total de participants que l'essai clinique vise à recruter.Cohorte
Éligibilité
Les chercheurs recherchent des patients correspondant à une certaine description appelée critères d'éligibilité : état de santé général ou traitements antérieurs du patient.Tout sexe
Le sexe biologique des participants éligibles à s'inscrire.À partir de 13 ans
Tranche d'âge des participants éligibles à participer.Volontaires sains non autorisés
Indique si les individus en bonne santé et ne présentant pas la condition étudiée peuvent participer.Conditions
Pathologie
Critères
Inclusion Criteria Patients must have: HIV infection. Stable weight. CD4+ cell count <200 cells/mm3. Life expectancy of at least 6 months. Parent or legal guardian to sign written, informed consent for patients < 18 years old. Exclusion Criteria Co-existing Condition: Patients with any of the following symptoms or conditions are excluded: Active opportunistic infection, requiring acute treatment. Malignancy (other than stable cutaneous Kaposi's sarcoma that does not require systemic chemotherapy). Diabetes mellitus or other conditions requiring special dietary restrictions. Body mass index (BMI) >= 29.0 kg/m2. Disorders or conditions that, in the treating clinician's opinion, may prevent adequate compliance with protocol requirements. Concurrent Medication: Excluded: Growth hormone. Megestrol acetate (Megace). Cyproheptadine (Periactin). Dronabinol (Marinol). Thalidomide. Anabolic steroids (e.g., nandrolone decanoate)(Deca-durabolin). Pharmacologic-dose corticosteroids (e.g., > 15 mg/day prednisone equivalent) NOTE: Men requiring testosterone replacement therapy for documented hypogonadism may be enrolled. Caloric nutritional supplements deemed by the clinician to promote weight gain or maintenance. Patients with the following prior condition are excluded: History of phenylketonuria. Prior Medication: Excluded within the past 2 weeks: Use of caloric nutritional supplements for more than 5 days deemed by the clinician to promote weight gain or maintenance. Excluded within the past 30 days: Growth hormone. Megestrol acetate (Megace). Cyproheptadine (Periactin). Dronabinol (Marinol). Thalidomide. Anabolic steroids (e.g., nandrolone decanoate)(Deca-durabolin) Pharmacologic-dose corticosteroids (e.g., > 15 mg/day prednisone equivalent). NOTE: Men requiring testosterone replacement therapy for documented hypogonadism may be enrolled.
Plan de l'étude
Découvrez tous les traitements administrés dans cette étude, leur description détaillée et ce qu'ils impliquent.3 groupes d'intervention sont désignés dans cette étude
Cette étude ne comporte pas de groupe placebo.
Groupes de traitement
Centres d'étude
Ce sont les hôpitaux, cliniques ou centres de recherche où l'essai est conduit. Vous pouvez trouver le site le plus proche de vous ainsi que son statut.Cette étude comporte 17 sites
Community Consortium / UCSF
San Francisco, United StatesOuvrir Community Consortium / UCSF dans Google MapsDenver CPCRA / Denver Public Hlth
Denver, United StatesWashington Reg AIDS Prog / Dept of Infect Dis
Washington D.C., United StatesAIDS Research Consortium of Atlanta
Atlanta, United States