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TerminatedNo phase

Study of Pregnancy And Neonatal Health (SPAN)

Key facts

Who runs it
Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
Where
Birmingham, Chapel Hill, Durham, Falls Church, Murray, New Orleans, Philadelphia, and Salt Lake City, United StatesSee the 8 sites
Trial code
Status
Terminated
People taking part
304 people enrolled
Started
20 Jan 2023
Ended
16 Dec 2024
Type of study
Interventional, 7 groups
Treatments tested
  • Childbirth
Record updated
24 December 2025
Why it stopped
Low enrollment

Who can take part

Age
18 years and older
Sex
Women only
Healthy volunteers
Can take part

The registry criteria, word for word

Show all 19 criteriaShow less

Who can take part

  • Aim 3 (GDM randomized trial, TIME) inclusion criteria:
  • Women inclusion criteria:
  • Age ≥ 18 Years
  • Verified diagnosis of Gestational Diabetes Mellitus (GDM) with abnormal glucose levels*** or meeting other criteria for poor control, specifically any one of the following: Estimated fetal weight ≥90th percentile (LGA), Polyhydramnios, and or Demonstrate noncompliance or nonadherence as defined clinically, including missing visits, not keeping accurate log, etc; ***One or more elevated fasting blood glucoses OR three or more elevated post-prandial blood glucoses after receiving education about appropriate diet and lifestyle modification (e.g. physical activity)
  • Accurate gestational age as verified by ultrasound
  • Singleton gestation
  • English or Spanish speaker
  • Plans to deliver at the study site hospital
  • Ability to provide informed consent to be randomized to initiation of delivery

Who cannot take part

  • Previous stillbirth defined as fetal demise ≥ 20 weeks of gestation
  • Pregnancies with concurrent conditions and other indications for earlier delivery will also be excluded
  • Self-reported history of alcohol dependency disorder and/or other drug/substance dependency in the past year
  • Known infectious diseases associated with neonatal morbidity (e.g. malaria, cytomegalovirus, rubella, toxoplasmosis, syphilis or Zika virus)
  • Genetic disorders, aneuploidy and known major fetal anomalies
  • Pre-gestational diabetes*; *will be defined as diabetes diagnosis before pregnancy OR before 13 weeks of gestation with a documented fasting plasma glucose ≥ 126 mg/dL, random plasma glucose ≥ 200 mg/dL, 2 hour post glucose ≥ 200 mg/dL during an oral glucose tolerance test (75 g glucose load), or hemoglobin A1c ≥ 6.5%.110
  • Aim 3 (GDM randomized trial, TIME) exclusion criteria:
  • Teratogen exposure (e.g. cyclophosphamide, valproic acid, warfarin)
  • Fetal demise
  • Participation in another interventional study that influences management of labor and delivery or perinatal morbidity or mortality

Where in United States

  • University of Alabama at BirminghamBirmingham, United States
  • University of North Carolina, Chapel HillChapel Hill, United States
  • Duke University Perinatal Research CenterDurham, United States
  • Inova Fairfax HospitalFalls Church, United States
  • Intermountain HealthcareMurray, United States
  • Ochsner BaptistNew Orleans, United States
  • University of PennsylvaniaPhiladelphia, United States
  • University of UtahSalt Lake City, United States

About the trial

What the trial wants to find out

This study will conduct a randomized trial among women with gestational diabetes (GDM). Study of Pregnancy And Neonatal health (SPAN), TIMing of dElivery (TIME) is a randomized trial that will recruit up to 3,450 pregnant women with uncontrolled GDM and randomize the timing of their delivery. Women with GDM who are approached for the trial and are found eligible but do not consent to participating in randomization for delivery will be asked to consent for chart review only (estimated additional n=3,000). The primary objective is to determine the best time to initiate delivery for GDM-complicated deliveries (defined as the time when risk of illness and death for the newborn is the lowest) between 37-39 weeks.

The 7 groups in the trial

  • Intervention Arm 1Treatment being tested

    Intervention Arm 1 Experimental Initiation of Delivery by induction or planned cesarean at 37 weeks 0-2 days.

    Treatment: Childbirth

  • Intervention Arm 2Treatment being tested

    Intervention Arm 2 Experimental Initiation of Delivery by induction or planned cesarean at 37 weeks 3-5 days.

    Treatment: Childbirth

  • Intervention Arm 3Treatment being tested

    Initiation of Delivery by induction or planned cesarean at 37 weeks 6 days to 38 weeks and 1 day.

    Treatment: Childbirth

  • Intervention Arm 4Treatment being tested

    Intervention Arm 4 Experimental Initiation of Delivery by induction or planned cesarean at 38 weeks 2-4 days.

    Treatment: Childbirth

  • Intervention Arm 5Treatment being tested

    Initiation of Delivery by induction or planned cesarean at 38 weeks 5 days to 39 weeks and 0 days.

    Treatment: Childbirth

  • Intervention Arm 6Treatment being tested

    Intervention Arm 6 Experimental Initiation of Delivery by induction or planned cesarean at 39 weeks 1-3 days.

    Treatment: Childbirth

  • Intervention Arm 7Treatment being tested

    Intervention Arm 7 Experimental Initiation of Delivery by induction or planned cesarean at 39 weeks 4-6 days.

    Treatment: Childbirth

Data and sources

Registry record
Listed on ClinicalTrials.gov.
Official title
Study of Pregnancy And Neonatal Health (SPAN): TIMing of dElivery (TIME) Trial
Record updated
24 December 2025