RecruitingNCT06282055
Trajectories in Insulin Sensitivity Across MEnstrual cycleS in Women With Type 1 Diabetes
Trajectories in Insulin Sensitivity Across Menstrual Cycles in Women With Type 1 Diabetes
Sponsor
DCB Research AG
Enrollment
350 participants
Start Date
Nov 20, 2025
Study Type
OBSERVATIONAL
Conditions
Summary
Standardized longitudinal data collection of diabetes management relevant factors in women with T1D (insulin requirements, glucose variability, nutritional information, and menstrual cycle information) to identify categories of cycle trajectories.
Eligibility
Sex: FEMALEMin Age: 18 YearsMax Age: 40 Years
Inclusion Criteria8
- Female sex
- Between 18 and 40 years at inclusion
- Menarche at least one year prior to study inclusion
- Regular menstrual cycle (at least one menstrual cycle in the last 40 days)
- Average menstrual cycle length between 21 and 38 days
- Difference in length between consecutive menstrual cycles of at most 7 days
- Living with type 1 diabetes or latent autoimmune diabetes in adults (LADA) for at least one year
- Actively using an AID system for their diabetes management at least six months prior to study inclusion
Exclusion Criteria7
- Regular hormonal intake (e.g. corticosteroids), except: insulin, stable thyroid substitution, and hormonal contraception
- Pregnancy until two months postpartum (ongoing or planned)
- Current breastfeeding (including pumping), as well as two months following complete cessation of breastfeeding and pumping
- Known Polycystic Ovary Syndrome (PCOS)
- Intake of glucocorticoid medication, agents affecting gastric emptying, oral anti-diabetic agents (Metformin) or SGLT-2 inhibitors or GLP-1-analogs
- Individuals with work patterns involving frequent shifts between night and day work (e.g., alternating night and day shifts on a weekly or similar basis).
- Participation in an interventional study within two months preceding and during the present study
Interventions
OTHERNo intervention
Observational prospective longitudinal data collection
Locations(1)
View Full Details on ClinicalTrials.gov
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NCT06282055
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