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NCT Number: NCT07293715

Permissive Versus Strict Intrapartum Glucose Management in Type 1 Diabetes (PRISM-T1D)

PRISM-TID is a single center non-inferiority randomized controlled trial of permissive intrapartum glucose management (intervention) versus strict intrapartum glucose management (standard of care) among pregnant individuals with type 1 diabetes (T1D) using hybrid closed loop therapy (HCL) who are admitted for labor management. Participants will be randomized in a 1:1 fashion to one of two intrapartum glycemic control options: permissive (70-140 mg/dL) or strict (70-110 mg/dL). The primary aim of this trial it to demonstrate that permissive intrapartum glucose management is not associated with an increased risk of neonatal dysglycemia compared with strict intrapartum glucose management.

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Key information

Age range

18 year and older

Sex eligibility

Female

Study type

Interventional

Phase

Phase 4

Primary location

The Ohio State University Wexner Medical Center OB/GYN Maternal and Fetal Medicine

Columbus, Ohio, 43210, United States

Location status: Recruiting

Location contact

Kartik Venkatesh, MD, PhD

CONTACT

[email protected]

614-293-4780

About this study

Type 1 Diabetes (T1D) affects approximately 0.5% of pregnancies in the US. Infants born to individuals with T1D are at increased risk of adverse pregnancy outcomes due to lack of glycemic control. Individuals with T1D are increasingly using hybrid closed loop therapy (HCL) for insulin delivery to achieve glycemic control. Current data highlight that less permissive intrapartum (while in labor) glycemic control is not associated with a increased risk of adverse pregnancy outcomes, including neonatal hypoglycemia and NICU admission. However, such data about permissive versus strict intrapartum glucose management has primarily been from pregnant individuals with type 2 diabetes or gestational diabetes who did not use HCL based insulin therapy. Pregnant individuals with diabetes who use HCL with continuous glucose monitoring and closed loop insulin delivery represent a unique population, and data from this population are needed to inform intrapartum obstetric management. The investigators hypothesize that permissive intrapartum glucose management using continuous glucose monitoring (70-140 mg/dL) will not be associated with neonatal dysglycemia measured as first mean neonatal glucose value within the first two hours of life compared with strict intrapartum glucose management or the current standard of care (70-110 mg/dL). The investigators will conduct a single center non-inferiority randomized controlled trial of permissive intrapartum glucose management (intervention) versus strict intrapartum glucose management (standard of care) among pregnant individuals with T1D using HCL who are admitted for labor management. The primary aim of this trial it to demonstrate that permissive intrapartum glucose management is not associated with an increased risk of neonatal dysglycemia (first neonatal blood glucose measured within 2 hours of life) compared with strict intrapartum glucose management. The investigators will secondarily examine the association between permissive versus strict intrapartum glucose with adverse neonatal outcomes, including neonatal hypoglycemia, neonatal hyperbilirubinemia, and NICU admission, patient satisfaction, and continuous glucose monitor (CGM) metrics.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Pregnant individuals
  • ≥ 18 years old
  • Type 1 diabetes
  • Intention for vaginal delivery and admitted to Labor and Delivery
  • Singleton, non-anomalous fetus
  • Gestational age greater than or equal to 35 weeks gestation.
  • Cervical dilation is less than 6 cm.
  • Delivering at the study institution

Exclusion criteria

  • Scheduled cesarean delivery
  • Cervical dilation ≥ 6 cm on presentation to L&D
  • Receipt of antenatal corticosteroids within 7 days of randomization
  • Fetal demise
  • Major fetal anomaly (attached)
  • Multiple gestation
  • Non-English speaking

Treatment and study plan

Insulin

Drug

Participants will be randomized in a 1:1 fashion to one of two intrapartum glycemic control options: permissive (70-140 mg/dL) or strict (70-110 mg/dL). Participants and clinicians will be unblinded. Once randomized, an order set will be entered into the EMR that will alert pharmacy and nursing colleagues to the appropriate intrapartum glycemic control protocol.

Dexcom continuous glucose monitor

Device

Patients will be asked to wear an optional Continuous Glucose Monitor (CGM) to utilize during labor for research purposes. The CGM will be removed prior to hospital discharge and data will be extracted by trained research personnel. All participants already utilize a CGM device as part of standard of care as part of Hybrid Closed Loop (HCL) therapy. No clinical decisions will be made based upon data from the research CGM device. This data will not be extracted until after hospital discharge.

Primary outcomes

  1. Mean of first neonatal blood glucose (continuous, mean with standard deviation)

    Time frame: From birth to 2 hours after birth

    The first heel stick neonatal blood glucose (mg/dL) will be obtained within the first two hours of life utilizing a hospital-grade glucometer. This will be recorded in the electronic medical record and abstracted at study conclusion. The mean of these will be utilized as the primary outcome. A heel stick neonatal blood glucose in the first two hours of life is current standard of care for all infants of diabetic individuals.

Secondary outcomes

  1. Neonatal C-peptide (continuous, mean with standard deviation)

    Time frame: At birth

    Umbilical cord C-peptide levels will be analyzed from cord blood collected at the time of delivery.

  2. Neonatal hypoglycemia

    Time frame: At birth, up to 24 hours

    Neonatal hypoglycemia: blood glucose < 40mg/dl in birth to 4 hours of life, < 45mg/dl in 4-24 hours of life, and < 50mg/dl after 24 hours of life, or need for oral or IV glucose therapy.

  3. Neonatal hyperbilirubinemia

    Time frame: Within the first 48 hours after birth

    Neonatal jaundice requiring phototherapy

  4. NICU admission

    Time frame: Within the first 48 hours after birth

    Admitted to NICU during delivery admission

  5. Birth experience satisfaction per Birth Satisfaction Survey-Revised (BSS-R) (continuous, mean with standard deviation)

    Time frame: Day 1 through study completion (at hospital discharge), up to 4 weeks

    The Birth Satisfaction Survey-Revised (BSS-R) is a validated patient satisfaction survey describing L&D birthing experiences. This survey will be administered at any time during their postpartum admission. This measure will be analyzed as a continuous mean score.

  6. Maternal IV insulin maximum dose and duration

    Time frame: Day 1 through study completion, up to 4 weeks

    Maternal IV insulin maximum IV insulin dose (units) and duration (hours) will be measured as continuous variables (mean and SD).

  7. Maternal Hypoglycemia

    Time frame: Day 1 through study completion, up to 4 weeks

    Maternal blood glucose less than 70 mg/dL, as measured by capillary blood glucose via hospital-grade glucometer.

Study contacts

Contact information is provided by the study sponsor or research team.

Anna Brewton, MD

CONTACT

[email protected]

614-293-8045

Sponsors and collaborators

Lead sponsor

Ohio State University

Other

Registry information

Acronym: PRISM-T1D

Important dates

Study start
2026
Primary completion
2027
Study completion
2027
First posted
Dec 19, 2025
Registry last updated
Apr 29, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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