Continuous Glucose Monitoring in New Mothers With Type 1 Diabetes

Continuous Glucose Monitoring During Breastfeeding or Formula Feeding in New Mothers With Type 1 Diabetes

Status

Completed

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT02898428

Enrollment

Registered

2016-09-13

Start date

2016-04-30

Completion date

2018-04-30

Last updated

2018-04-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Breastfeeding, Hypoglycemia

Brief summary

With appropriate day-time carbohydrate intake and insulin dose, the 24 hour glucose levels and prevalence of night-time hypoglycaemia are comparable in breastfeeding new mothers and formula feeding new mothers with type 1 diabetes at the second after delivery diabetes control compared with the first after delivery diabetes control at Steno Diabetes Center.

Interventions

DEVICEContinuous glucose monitoring (CGM)

Study design

Observational model

CASE_CONTROL

Time perspective

PROSPECTIVE

Eligibility

Sex/Gender

FEMALE

Age

18 Years to 45 Years

Healthy volunteers

Inclusion criteria

* Age between 18 and 45 years. * Delivery of a single infant. * Proficiency in Danish to read and understand the patient information sheet, questionnaires and to converse with the diabetes caregivers.

Exclusion criteria

* A diagnosis with severe mental or psychiatric barriers or a concurrent disease on the decision of the principal investigator

Design outcomes

Primary

Measure	Time frame
Hypoglycemia	Night-time 8 hours

Countries

Denmark

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 4, 2026