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NCT06883344Recruiting

Automated Insulin for Management of Intrapartum Glycemia

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

Source: ClinicalTrials.gov · Last updated 13 Jul 2026

Brief summary (registry, in English)

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.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
150 (estimated)
First submitted
12 Mar 2025
Start date
5 Dec 2025
Primary completion date
31 Dec 2028
Lead sponsor
University of California, San Francisco
NCT number
NCT06883344

What you commit to

  • Study type: Interventional
  • Planned participants: 150
  • From 5 Dec 2025 to the primary completion date, 31 Dec 2028
  • 3 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Physical or psychological disease likely to interfere with the conduct of the study and/or the ability to participate in own healthcare

Lab values

  • Use of medications known to interfere with glucose metabolism

Other

  • Multifetal gestation
  • Planned cesarean delivery
  • Intrauterine fetal demise

Who the study is looking for

  • 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

Age in the registry: 18 years to 55 years · Sex: Female · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (3)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
University of California, Los Angeles
Coordinator of this site? Confirm its status
Los AngelesUnited StatesRecruiting
University of California San Diego
Coordinator of this site? Confirm its status
San DiegoUnited StatesRecruiting
University of California San Francisco
Coordinator of this site? Confirm its status
San FranciscoUnited StatesRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.