Gestational diabetes & diabetes in pregnancy

Intrapartum and Early Postpartum Use of Automated Insulin Delivery in Type 1 Diabetes: A Prespecified Analysis of the CIRCUIT Randomized Controlled Trial

Diabetes CarePublished Secondary analysis of the CIRCUIT randomised trial

Primary result · % time in range 63-140 mg/dLResult — go to the resultMean adjusted difference 13.2 percentage points 95% CI 5.2–21.2

Authors' conclusion

Use of this closed-loop system resulted in superior intrapartum and early postpartum glycemia compared with standard care without safety concerns.

Study context

Population
Pregnant women with T1D, intrapartum and early postpartum
Comparison
Control-IQ closed loop vs standard care
  • Closed loopn = 44
Primary endpoint
% time in pregnancy-specific glucose range (63-140 mg/dL) by CGM
Follow-up
24 h prior to childbirth
Methodological detailsprespecified analysis
  • Prespecified analysis

Primary result

% time in range 63-140 mg/dL · 24 h before delivery

Mean adjusted difference

13.2 percentage points

95% CI 5.2–21.2

By group

Closed loopvs Standard care
mean adjusted difference 13.2 percentage points (95% CI 5.2–21.2)

As reported in the abstract

Secondary outcomes

Key secondary: % time <70 mg/dL · first postpartum week

mean adjusted difference (percentage points) −1.8 (−0.9 to −2.7)

Intrapartum IV insulin use

P < 0.001

Continued closed loop intrapartum · 24 h before delivery
89% · 39 of 44

Safety

Intrapartum intravenous insulin use

P < 0.001

OutcomeClosed loopStandard care
Maternal severe hypoglycemia · postpartum— not stated in the abstractone episode events

— not stated in the abstract

Maternal severe hypoglycemia · postpartum

No maternal severe hypoglycemia occurred in the closed-loop group

Diabetic ketoacidosis

No diabetic ketoacidosis occurred in either group

Original publication

Intrapartum and Early Postpartum Use of Automated Insulin Delivery in Type 1 Diabetes: A Prespecified Analysis of the CIRCUIT Randomized Controlled Trial. Diabetes Care. Published 27 May 2026. doi:10.2337/dc26-0470

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