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RECRUITINGOBSERVATIONAL

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

Important: This information is not medical advice. Talk to your doctor about whether a clinical trial is right for you.

About This Trial

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.

Who May Be Eligible (Plain English)

Who May Qualify: - 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 Who Should NOT Join This Trial: - 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 Always talk to your doctor about whether this trial is right for you.

Original Eligibility Criteria

View original clinical language
Inclusion criteria: * 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 criteria: * 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

Treatments Being Tested

OTHER

No intervention

Observational prospective longitudinal data collection

Locations (1)

DCB Research AG
Bern, Switzerland