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CompletedNCT04520971

Closed-loop Insulin Delivery in Pregnant Women With Type 1 Diabetes

Closed-loop Insulin Delivery in Pregnant Women With Type 1 Diabetes: a Randomized Controlled Trial: the CRISTAL Study

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
95 (actual)
Sponsor
Universitaire Ziekenhuizen KU Leuven · Academic / Other
Sex
Female
Age
18 Years – 45 Years
Healthy volunteers
Not accepted

Summary

Multi-centric open-label randomized controlled trial (RCT) with 11 Belgian centers and one Dutch center in pregnant women with type 1 diabetes to assess safety, efficacy, feasibility and cost-effectiveness of 780 MiniMed Medtronic hybrid closed-loop insulin system (intervention group) compared to standard of care therapy (control group).

Detailed description

Women will be recruited with a singleton pregnancy up to 12 weeks gestation. Participants will be randomized 1/1 to 780 pump or standard of care (continue with current treatment of insulin pump without closed-loop or multiple daily insulin injections). Participants will be stratified according to study center, baseline Hba1c, and method of insulin delivery (pump or injections). Participants will be followed-up till delivery. To account for differences in the type of continuous glucose monitoring (CGM) used between the intervention group and the control group, the same CGM system as in the 780 insulin pump group (Guardian™ Sensor 3 and once available the Guardian 4 sensor) will be used in a blinded manner in the control group to collect CGM data during at least four different time points in pregnancy: at 14-17 weeks, 20-23 weeks, 26-29 weeks and 33-36 weeks.

Conditions

Interventions

TypeNameDescription
DEVICE780G780G closed-loop insulin delivery system (Medtronic)
DEVICEstandard of carecontinue with standard of care treatment (pump without closed-loop or MDI)

Timeline

Start date
2021-01-15
Primary completion
2023-04-30
Completion
2023-05-10
First posted
2020-08-20
Last updated
2024-12-10

Locations

12 sites across 2 countries: Belgium, Netherlands

Source: ClinicalTrials.gov record NCT04520971. Inclusion in this directory is not an endorsement.