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