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Treating Prediabetes in the First Trimester

9. oktober 2018 oppdatert av: Hilary Roeder, MD, University of California, San Diego

Treating Prediabetes in the First Trimester: A Randomized Controlled Trial

The investigators plan to study a sample of women with prediabetes (diagnosed by Hemoglobin A1c (HbA1c) 5.7-6.4% or fasting plasma glucose (FPG) 92-125 mg/dL) in the first trimester of pregnancy, and patients will be randomized to first trimester or third trimester treatment; the first trimester group will receive intervention immediately upon diagnosis of prediabetes whereas the third trimester group will receive only routine prenatal care until 28 weeks at which time they will receive intervention.

Intervention is defined as:

  • diabetes education
  • blood glucose monitoring
  • medications as needed
  • growth ultrasounds
  • antenatal testing

The primary outcome is umbilical cord C-Peptide >90th percentile. Secondary outcomes include neonatal fat mass at delivery, infant weight-for-length at 12 months of age, maternal gestational weight gain, and biomarkers (chemicals) measured in the placenta and the baby's umbilical cord blood.

The investigators hypothesize that women who undergo the above intervention in the first trimester will deliver significantly fewer neonates with umbilical cord C-Peptide >90th percentile, and that the neonates will have lower fat mass, and weight-for-length at 12 months. The investigators further hypothesize that a greater proportion of patients undergoing first trimester intervention will have appropriate maternal gestational weight gain as defined by the Institute of Medicine, and a greater proportion will return to prepregnancy weight within 12 months.

Studieoversikt

Status

Fullført

Intervensjon / Behandling

Detaljert beskrivelse

The primary aim of the proposed research is to demonstrate that promoting a normoglycemic intrauterine milieu in women with prediabetes diagnosed in the first trimester of pregnancy with a Hemoglobin A1c (HbA1c) 5.7-6.4% or fasting plasma glucose (FPG) 92-125 mg/dL will decrease the accumulation of fetal white adipose tissue and development of infant/child obesity during the first year of life. This project is built upon the hypothesis that pregnant subjects with prediabetes randomized in the first trimester of pregnancy to strict glycemic control and pharmacotherapy as needed will have less fetal adiposity and adverse neonatal outcomes than those who receive the diagnosis of prediabetes but do not initiate care until the third trimester.

In the proposed study, 240 women meeting the above criteria for prediabetes at ≤ 15w0d gestation will be randomized to either first trimester or third trimester treatment. Each group will have diabetes education, initiate blood glucose monitoring, begin pharmacotherapy as needed (per established protocol), undergo growth ultrasounds, and antenatal testing. The first trimester arm will receive the above interventions immediately upon diagnosis of prediabetes whereas the third trimester arm will receive only routine prenatal care until 28 weeks at which time they will begin education and treatment. Both groups will be treated identically from 28 weeks until delivery.

In the 2013 the National Institutes of Health (NIH) Gestational Diabetes (GDM) Consensus Conference, the panel was concerned about adopting criteria that would increase prevalence of GDM (i.e. first trimester treatment) without first demonstrating improved outcomes. The results of this proposed trial, will allow us to fill key research gaps; this is the first prospective trial to evaluate the International Associations of Diabetes in Pregnancy Study Groups (IADPSG) recommendations for screening and diagnosing prediabetes in the first trimester.

Findings from this research will quantify the maternal and neonatal benefits and harms of treating women with prediabetes from early pregnancy. Additionally, the cohort of neonates that will result from this study can be followed into childhood to evaluate whether first trimester treatment has benefits beyond those anticipated at birth and may decrease the long-term incidence of obesity and diabetes.

Studietype

Intervensjonell

Registrering (Faktiske)

202

Fase

  • Ikke aktuelt

Kontakter og plasseringer

Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.

Studiesteder

    • California
      • San Diego, California, Forente stater, 92103
        • UC San Diego Health System

Deltakelseskriterier

Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.

Kvalifikasjonskriterier

Alder som er kvalifisert for studier

18 år og eldre (Voksen, Eldre voksen)

Tar imot friske frivillige

Ja

Kjønn som er kvalifisert for studier

Hunn

Beskrivelse

Inclusion Criteria:

  • Pregnant women age 18 and above
  • Any ethnic background
  • English- or Spanish-speaking
  • Planned prenatal care/delivery at The University of California, San Diego's Hillcrest Hospital
  • Singleton pregnancy
  • Prediabetes diagnosed prior to 15w0d with HbA1c 5.7-6.4% or FPG 92-125 mg/dL

Exclusion Criteria:

  • Known Type 2 Diabetes (T2DM)
  • T2DM diagnosed with first trimester screening
  • Patients with known maternal/fetal indications for delivery <36w0d
  • Patients presenting for care after 15w0d

Studieplan

Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.

Hvordan er studiet utformet?

Designdetaljer

  • Primært formål: Behandling
  • Tildeling: Randomisert
  • Intervensjonsmodell: Parallell tildeling
  • Masking: Enkelt

Våpen og intervensjoner

Deltakergruppe / Arm
Intervensjon / Behandling
Eksperimentell: First Trimester Treatment of Prediabetes

Patients randomized to first trimester treatment will receive the following intervention immediately initiated upon diagnosis of prediabetes at <15 weeks 0 days gestation

  • diabetes education
  • blood glucose monitoring
  • medications as needed per California Diabetes and Pregnancy established protocol
  • growth ultrasounds
  • antenatal testing

Standardized treatment of prediabetes per California Diabetes and Pregnancy Program "Sweet Success"

  • diabetes education
  • blood glucose monitoring
  • medications as needed per California Diabetes and Pregnancy established protocol
  • growth ultrasounds
  • antenatal testing
Aktiv komparator: Third Trimester Treatment of Prediabetes

Patients randomized to third trimester treatment will receive the following intervention to be initiated at 28 weeks of gestation

  • diabetes education
  • blood glucose monitoring
  • medications as needed per California Diabetes and Pregnancy established protocol
  • growth ultrasounds
  • antenatal testing

Standardized treatment of prediabetes per California Diabetes and Pregnancy Program "Sweet Success"

  • diabetes education
  • blood glucose monitoring
  • medications as needed per California Diabetes and Pregnancy established protocol
  • growth ultrasounds
  • antenatal testing

Hva måler studien?

Primære resultatmål

Resultatmål
Tidsramme
Umbilical Cord C-Peptide >90th percentile
Tidsramme: 1 day (Collected at the time of delivery)
1 day (Collected at the time of delivery)

Sekundære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Neonatal fat mass
Tidsramme: Within 48 hours of delivery
Neonatal fat mass will be measured using an anthropometric model using weight, length, and flank skinfold thickness.
Within 48 hours of delivery
Adherence to the Institute of Medicine (IOM) guidelines for gestational weight gain
Tidsramme: Weight gain will be measured from immediately preconception until delivery
The IOM recommends that underweight women (BMI<18.5kg/m2) gain 28-40lbs, normal women (BMI 18.5-24.9 kg/m2) gain 25-35lbs, overweight women (BMI 25.0-29.9 kg/m2) gain 15-25lbs and obese women (BMI≥30 kg/m2) gain 11-20 lbs.
Weight gain will be measured from immediately preconception until delivery
Return to prepregnancy weight
Tidsramme: After 1 year post delivery
After 1 year post delivery

Andre resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
birthweight
Tidsramme: At delivery
At delivery
birthweight percentile
Tidsramme: At delivery
At delivery
Infant gender
Tidsramme: At delivery
At delivery
Ponderal index
Tidsramme: At delivery
Weight/length^3
At delivery
Neonatal Intensive Care Unit (NICU) Admission
Tidsramme: Within 10 days after birth
Within 10 days after birth
Infant weight-for-length
Tidsramme: 6 months and 12 months after delivery
6 months and 12 months after delivery
Need for pharmacotherapy to control hyperglycemia
Tidsramme: From 5 weeks gestation until time of delivery
From 5 weeks gestation until time of delivery
Birth trauma
Tidsramme: At delivery
Shoulder dystocia, brachial plexus injury
At delivery
Mode of delivery
Tidsramme: At delivery
Spontaneous delivery, operative vaginal delivery, cesarean delivery
At delivery
Indication for delivery
Tidsramme: At delivery
At delivery
Total gestational weight gain
Tidsramme: From immediately preconception until delivery
From immediately preconception until delivery
Postpartum weight retention
Tidsramme: Within 1 year of delivery
Within 1 year of delivery
Diagnosis of Preeclampsia
Tidsramme: From 20 weeks gestation until 6 weeks postpartum
From 20 weeks gestation until 6 weeks postpartum

Samarbeidspartnere og etterforskere

Det er her du vil finne personer og organisasjoner som er involvert i denne studien.

Etterforskere

  • Hovedetterforsker: Hilary A Roeder, MD, UC San Diego Health System
  • Hovedetterforsker: Gladys A Ramos, MD, UC San Diego Health System
  • Hovedetterforsker: Thomas R Moore, MD, UC San Diego Health System

Publikasjoner og nyttige lenker

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Generelle publikasjoner

Studierekorddatoer

Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.

Studer hoveddatoer

Studiestart

1. juli 2013

Primær fullføring (Faktiske)

1. juni 2016

Studiet fullført (Faktiske)

15. juni 2017

Datoer for studieregistrering

Først innsendt

15. august 2013

Først innsendt som oppfylte QC-kriteriene

20. august 2013

Først lagt ut (Anslag)

21. august 2013

Oppdateringer av studieposter

Sist oppdatering lagt ut (Faktiske)

10. oktober 2018

Siste oppdatering sendt inn som oppfylte QC-kriteriene

9. oktober 2018

Sist bekreftet

1. oktober 2018

Mer informasjon

Denne informasjonen ble hentet direkte fra nettstedet clinicaltrials.gov uten noen endringer. Hvis du har noen forespørsler om å endre, fjerne eller oppdatere studiedetaljene dine, vennligst kontakt register@clinicaltrials.gov. Så snart en endring er implementert på clinicaltrials.gov, vil denne også bli oppdatert automatisk på nettstedet vårt. .

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