Open Actively Recruiting

Automated Insulin for Management of Intrapartum Glycemia

About

Brief Summary

The goal of this clinical trial is learn if automated insulin delivery (AID) systems can be used for glucose management during labor/delivery for pregnant people with type 1 diabetes (T1D). The main questions this study aims to answer are

  • What are the neonatal glycemic outcomes with use of AID systems during labor/delivery?
  • Do patients report higher birth satisfaction with use of AID systems during labor/delivery?
  • Are glycemic parameters like time-in-range (TIR) better with use of AID systems during labor/delivery?

Researchers will compare AID systems to intravenous (IV) insulin (the current standard of care for glucose management during labor/delivery) by randomly assigning participants to one or the other.

Primary Purpose
The main objective of the intervention(s) being evaluated by the clinical trial. Learn more
Treatment
Study Type
The nature of the investigation or investigational use for which clinical study information is being submitted. Learn more
Interventional
Phase
N/A

Eligibility

Gender
Female
Healthy Volunteers
No
Minimum Age
18 Years
Maximum Age
55 Years

Inclusion Criteria:

  • Currently pregnant at ≥ 34 weeks
  • Known diagnosis of type 1 diabetes ≥ 1 year
  • Use of commercially available AID system since at least 28 weeks gestation
  • Singleton pregnancy
  • English- or Spanish-speaking

Exclusion Criteria:

  • Multifetal gestation
  • Planned cesarean delivery
  • Use of medications known to interfere with glucose metabolism
  • Intrauterine fetal demise
  • Physical or psychological disease likely to interfere with the conduct of the study and/or the ability to participate in own healthcare
Study Stats
Protocol No.
25-2274
Category
Endocrine and Metabolic Disorders
Pregnancy
Principal Investigator
Christina S. Han, MD
Christina S. Han, MD
Maternal and Fetal Medicine
Christina S. Han, MD
Contact
  • Kimberly Huynh
Location
  • UCLA Santa Monica
  • UCLA Westwood
For Providers
NCT No.
NCT06883344
For detailed technical eligibility, visit ClinicalTrials.gov.