Glycemic Profiles And Insulin Delivery Across The Menstrual Cycle In Women With Type 1 Diabetes
Trial Snapshot
- Phase
- Not Applicable
- Status
- Completed
- Sponsor
- University of Virginia
- Enrollment
- 37
- Locations
- 1
- Primary Endpoint
- Insulin sensitivity computed using a Kalman filter-base algorithm embedding a model of glucose-insulin dynamics.
Study Overview
Brief Summary
This is an observational study. Forty females with type 1 diabetes (age 18-40) using a continuous glucose monitor and an insulin pump will be enrolled for a 3-month data collection. Study participants will include free-cycling females and females following oral contraceptive therapy. All study appointments may be completed virtually.
Detailed Description
Females, age 18-40 y.o., diagnosed with type 1 diabetes and currently using an insulin pump, will be provided a study continuous glucose monitor (CGM) in order to collect 3 full menstrual cycle data within 180 days. Enrollment may last from 3-5 months. Study participants will include free-cycling females and females following oral contraceptive therapy. Study CGMs and activity trackers will be provided for the entire data collection period. During data collection, all participants will be asked to record meals consumed and free-cycling females will be asked to confirm ovulation by means of study-provided ovulation kits. The Clue app will be recommended to study participants to record dates of beginning of menses and ovulation (if applicable).
Study Design
- Study Type
- Observational
- Observational Model
- Other
- Time Perspective
- Prospective
Eligibility Criteria
- Ages
- 18 Years to 40 Years (Adult)
- Sex
- Female
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- •Type 1 diabetes for at least 12 months
- •Use of glucose sensor in the last 6 months
- •Use of insulin pump in the last 6 months
- •Age ≥18 to ≤40 years
- •HbA1c ≤8.5% if measured at screening or available from historical medical report performed within the last 6 months; in absence of a valid HbA1c measurement, average blood glucose estimated from CGM data to be approximately 200 mg/dL or less
- •Absence of perimenopausal/menopausal symptoms
- •Willingness to keep track of beginning of menstrual cycle
- •Willingness to keep track of ingested carbohydrates
- •Willingness to not become pregnant during study participation
- •Regularly menstruating (at least every month with no missed cycles)
- •Only free-cycling participants: willingness to use ovulation kits to confirm ovulation
- •Only participants under oral contraceptive therapy: use of monophasic pill, with 3 weeks of active pill and 1 week of placebo
- •Willingness to use the study Dexcom G6 during the study
- •Participants must have Internet access and a computer system that meets the requirements for uploading the study equipment
Exclusion Criteria
- •Pregnancy
- •Hormonal birth control therapy except monophasic pill contraceptive
- •Polycystic ovary syndrome (PCOS) diagnosis
- •Current use of steroids
- •Concurrent use of any non-insulin glucose-lowering agent (including GLP-1 agonists, pramlintide, DPP-4 inhibitors, SGLT-2 inhibitors, sulfonylureas, metformin)
- •Uncontrolled thyroid disease
- •Active fertility treatment
- •Concomitant disease or condition that may compromise patient safety or ability to follow the protocol including: planned or current dialysis treatment; moderate to advanced nephropathy; known or suspected allergy to medical grade adhesives.
- •Severe hypoglycemia or diabetes ketoacidosis (DKA) in the previous 6 months
Outcomes
Primary Outcomes
Insulin sensitivity computed using a Kalman filter-base algorithm embedding a model of glucose-insulin dynamics.
Time Frame: 3 months
Primary Variable
Secondary Outcomes
No secondary outcomes reported
Investigators
Chiara Fabris, PhD
Primary Investigator
University of Virginia