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Treating Prediabetes in the First Trimester

9. oktober 2018 opdateret af: 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.

Studieoversigt

Status

Afsluttet

Intervention / Behandling

Detaljeret 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.

Undersøgelsestype

Interventionel

Tilmelding (Faktiske)

202

Fase

  • Ikke anvendelig

Kontakter og lokationer

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

Studiesteder

    • California
      • San Diego, California, Forenede Stater, 92103
        • UC San Diego Health System

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

18 år og ældre (Voksen, Ældre voksen)

Tager imod sunde frivillige

Ja

Køn, der er berettiget til at studere

Kvinde

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

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: Enkelt

Våben og indgreb

Deltagergruppe / Arm
Intervention / Behandling
Eksperimentel: 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

Hvad måler undersøgelsen?

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
Foranstaltningsbeskrivelse
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
Foranstaltningsbeskrivelse
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

Samarbejdspartnere og efterforskere

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

Efterforskere

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

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. juli 2013

Primær færdiggørelse (Faktiske)

1. juni 2016

Studieafslutning (Faktiske)

15. juni 2017

Datoer for studieregistrering

Først indsendt

15. august 2013

Først indsendt, der opfyldte QC-kriterier

20. august 2013

Først opslået (Skøn)

21. august 2013

Opdateringer af undersøgelsesjournaler

Sidste opdatering sendt (Faktiske)

10. oktober 2018

Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier

9. oktober 2018

Sidst verificeret

1. oktober 2018

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 .

Kliniske forsøg med Treatment of Prediabetes

3
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