Garcinia Mangostana Extracts in the Management of Weight Loss
Sleutelwoorden
Abstract
Omschrijving
After the screening visit for the evaluation of the inclusion / exclusion criteria and sign informed consent(Visit 1), each patient will be randomized (Visit 2; Time 0; Baseline) (1: 1) to receive two different treatment for the duration of 26 weeks:
1. low-calorie balanced diet consistent exercise (control group)
2. balanced low-calorie diet and regular exercise in combination with the assumption of Garcinia mangostana (treatment group)
Throughout the duration of the study, every eight weeks, unless otherwise indicated from the specialists, for each subject was expected a nutritional and an endocrinological visit with a anthropometric parameter check (body composition) and compliance to therapy (dietary / physical activity diary).
Also a bood sample test was performed to evaluate electrocardiogram, lipid profile, glucose tolerance, hormonal parameters, inflammatory and bone markers.
Datums
Laatst geverifieerd: | 05/31/2016 |
Eerste ingediend: | 06/22/2016 |
Geschatte inschrijving ingediend: | 06/29/2016 |
Eerst geplaatst: | 07/05/2016 |
Laatste update ingediend: | 08/29/2016 |
Laatste update geplaatst: | 08/30/2016 |
Werkelijke startdatum van het onderzoek: | 10/31/2015 |
Geschatte primaire voltooiingsdatum: | 04/30/2016 |
Geschatte voltooiingsdatum van het onderzoek: | 04/30/2016 |
Conditie of ziekte
Interventie / behandeling
Dietary Supplement: Garcinia mangostana (treatment group)
Behavioral: Control group
Fase
Armgroepen
Arm | Interventie / behandeling |
---|---|
Active Comparator: Garcinia mangostana (treatment group) Balanced low-calorie diet and regular exercise in combination with integration | Dietary Supplement: Garcinia mangostana (treatment group) |
Other: Control group balanced low-calorie diet and regular exercise | Behavioral: Control group |
Geschiktheidscriteria
Leeftijden die in aanmerking komen voor studie | 18 Years Naar 18 Years |
Geslachten die in aanmerking komen voor studie | All |
Accepteert gezonde vrijwilligers | Ja |
Criteria | Inclusion Criteria: - Obesity: BMI >35 kg/m2. - Stable medical therapy for comorbidities from at least 6 months Exclusion Criteria: - Hormonal replacement therapy - Hyperprolactinaemia and /or other endocrine hypothalamic-pituitary diseases (empty sella syndrome and expansive pituitary disorders evaluated by MRI) - Any other condition that medical judgment precludes patient safety |
Resultaat
Primaire uitkomstmaten
1. Weight loss - Kg reduction [26 weeks]
Secundaire uitkomstmaten
1. Insulin sensitivity assessed by the homeostatic model assessment (HOMA-IR) [26 weeks]
2. Lipid profile by serum biochemistry [26 weeks]
3. Abdominal obesity measured by waist circumference [26 weeks]
4. Body composition by Dexa parameters [26 weeks]
5. Changes in microalbuminuria by unin analysis [26 weeks]