Summary

Eligibility
for females ages 13-55 (full criteria)
Location
at UCSF
Dates
study started
completion around
Principal Investigator
by Ivonne Verduzco, MD (ucsf)

Description

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.

Official Title

Automated Insulin for Management of Intrapartum Glycemia (AIMING): a Randomized Clinical Trial

Keywords

Type 1 Diabetes (T1D), Pregnancy, Pre-Gestational Diabetes, Intrapartum glycemic management, Neonatal hypoglycemia, Perinatal care, Diabetes in pregnancy, Gestational Diabetes, Diabetes Mellitus, Insulin, Globin Zinc Insulin, Automated insulin delivery (AID) system, Intravenous (IV) insulin

Eligibility

You can join if…

Open to females ages 13-55

  • Known diagnosis of type 1 diabetes ≥ 1 year
  • Current use of commercially available AID system ≥ 6 months
  • Currently pregnant at ≥ 34 weeks
  • Singleton pregnancy
  • English- or Spanish-speaking

You CAN'T join if...

  • 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

Location

  • University of California, San Francisco
    San Francisco California 94143 United States

Lead Scientist at University of California Health

Details

Status
not yet accepting patients
Start Date
Completion Date
(estimated)
Sponsor
University of California, San Francisco
ID
NCT06883344
Study Type
Interventional
Participants
Expecting 150 study participants
Last Updated