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Adipokines in Obese Adolescents With Insulin Resistance

23. april 2012 opdateret af: Maria Lola Evia-Viscarra, Hospital Regional de Alta Especialidad del Bajio

Inflammatory Mediators in Obese Adolescents With Insulin Resistance Following Metformin Treatment: Controlled Randomized Clinical Trial

The purpose of this study is to compare serum concentrations of inflammatory cytokines, interleukin 6 (IL-6), High-sensitivity C-reactive protein (hs-CRP), adiponectin, and tumour necrosis factor alpha (TNFα), before and after three months treatment with metformin in obese adolescents with insulin resistance (IR).

Studieoversigt

Status

Afsluttet

Betingelser

Detaljeret beskrivelse

The increased prevalence of obesity in pediatric patients is a public health problem particularly because of the difficulties involved with changing lifestyles. Current studies of obese children and adolescents show increased insulin resistance (IR) and chronic inflammatory states. These conditions increase the risk of disability and/or premature death.

The current treatment schemes for obese children are conservative and are focused on changing their lifestyles (exercise and dietary plans). However, metabolic conditions, such as IR, dyslipidemia, and inflammatory processes, are perpetuated.

Metformin is a biguanide that is used for adolescents with diabetes mellitus and polycystic ovarian syndrome. Several clinical trials with metformin for obese pediatric patients have observed decreases in IR, decreases in weight, and improvements in lipid metabolism.

Adipose tissue is not only an energy repository, but also plays an immunological role by the secretion of cytokines. Both overweight adults and adolescents show decreases in adiponectin levels and increases in tumor necrosis factor alpha (TNFα) and interleukin 6 (IL-6). IL-6 can stimulate the production of high-sensitivity C-reactive protein (hs-CRP), which is considered to be a risk marker for the development of cardiovascular disease.

Undersøgelsestype

Interventionel

Tilmelding (Faktiske)

31

Fase

  • Fase 4

Kontakter og lokationer

Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.

Studiesteder

    • Distrito Federal
      • México, Distrito Federal, Mexico, 06720
        • Hospital Infantil de Mexico Federico Gomez
    • Guanajuato
      • León, Guanajuato, Mexico, 37670
        • Hospital Regional de Alta Especialidad del Bajio

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

9 år til 18 år (Barn, Voksen)

Tager imod sunde frivillige

Ingen

Køn, der er berettiget til at studere

Alle

Beskrivelse

Inclusion Criteria:

  • Obesity defined as Body Mass Index (BMI) ≥ percentile 95
  • Tanner stage ≥ 2
  • Insulin resistance defined as Basal insulin > 15 µU/mL or Homeostasis Model Assessment index (HOMA) > 4.5
  • Patients' parents signed written consents when they and their adolescent children agreed to enroll

Exclusion Criteria:

  • Glucose intolerance
  • Diabetes mellitus (type 1 or 2)
  • Anemia (Hb < 10 g/dL)
  • Plasma creatinine > 1.4 mg/dL
  • Abnormal hepatic function
  • Any associated Disease (Pulmonary, Infection, Autoimmune Disease)
  • History of lactic acidosis

Studieplan

Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.

Hvordan er undersøgelsen tilrettelagt?

Design detaljer

  • Primært formål: Behandling
  • Tildeling: Randomiseret
  • Interventionel model: Parallel tildeling
  • Maskning: Firedobbelt

Våben og indgreb

Deltagergruppe / Arm
Intervention / Behandling
Eksperimentel: Metformin
Tablet of 500 mg metformin, oral every 12 hours (total metformin dose of 1 g/day) for 3 months.
Tablet of 500 mg metformin, oral every 12 hours (total metformin dose of 1 g/day) for 3 months.
Andre navne:
  • Dabex
Placebo komparator: Placebo
Tablet of 500 mg oral placebo every 12 hours for 3 months.
Tablet of 500 mg oral placebo every 12 hours for 3 months.

Hvad måler undersøgelsen?

Primære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Adiponectin
Tidsramme: baseline and 3 months
Change from baseline in Adiponectin after 3 months of treatment.
baseline and 3 months
High-sensitivity C-reactive Protein
Tidsramme: baseline and 3 months
Change from baseline in High-sensitivity C-reactive protein after 3 months of treatment.
baseline and 3 months
Interleukin 6
Tidsramme: baseline and 3 months
Change from baseline in Interleukin 6 after 3 months of treatment.
baseline and 3 months
Tumour Necrosis Factor Alpha
Tidsramme: baseline and 3 months
Change from baseline in Tumour necrosis factor alpha after 3 months of treatment.
baseline and 3 months

Sekundære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Fasting Plasma Glucose
Tidsramme: baseline and 3 months
Change from baseline in Fasting plasma glucose after 3 months of treatment.
baseline and 3 months
Fasting Insulin
Tidsramme: baseline and 3 months
Change from baseline in Fasting insulin after 3 months of treatment.
baseline and 3 months
Body Mass Index
Tidsramme: baseline and 3 months
Change from baseline in Body Mass Index after 3 months of treatment.
baseline and 3 months
Waist Circumference
Tidsramme: baseline and 3 months
Change from baseline in Waist circumference after 3 months of treatment.
baseline and 3 months

Samarbejdspartnere og efterforskere

Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.

Efterforskere

  • Ledende efterforsker: Maria L Evia-Viscarra, M.D., Hospital Regional de Alta Especialidad del Bajio
  • Studiestol: Edel R Rodea-Montero, Statistician, Hospital Regional de Alta Especialidad del Bajio
  • Studiestol: Evelia Apolinar-Jiménez, Nutrition, Hospital Regional de Alta Especialidad del Bajio
  • Studiestol: Leticia M García-Morales, M.D., Hospital Infantil de Mexico Federico Gomez
  • Studiestol: Constanza Leaños-Pérez, M.D., Hospital Infantil de Mexico Federico Gomez
  • Studiestol: Mireya Figueroa-Barrón, Chemestry, Hospital Infantil de Mexico Federico Gomez
  • Studiestol: Dolores Sánchez-Fierros, Chemestry, Hospital Infantil de Mexico Federico Gomez
  • Studiestol: Nathalie Muñoz-Noriega, Nutrition, Hospital Regional de Alta Especialidad del Bajio
  • Studiestol: Juan G Reyes-García, M.D., Escuela Superior de Medicina del IPN

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.

Generelle publikationer

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. januar 2007

Primær færdiggørelse (Faktiske)

1. december 2009

Studieafslutning (Faktiske)

1. marts 2010

Datoer for studieregistrering

Først indsendt

4. august 2011

Først indsendt, der opfyldte QC-kriterier

4. august 2011

Først opslået (Skøn)

5. august 2011

Opdateringer af undersøgelsesjournaler

Sidste opdatering sendt (Skøn)

27. april 2012

Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier

23. april 2012

Sidst verificeret

1. april 2012

Mere information

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 .

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