The goal is to establish the effect of oral inulin supplementation on continuous glucose monitoring (CGM) metrics and immunological parameters in adults with type 1 diabetes. The investigators will perform a double-blind, randomized, placebo-controlled trial in 2x38 participants to measure effects on CGM metrics, gut microbiome composition, residual beta cell and immunological parameters.
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Eligibility Criteria
Inclusion Criteria:
* A diagnosis of type 1 diabetes, as made by their primary clinician
* A time in range of \<80% in the last four weeks before screening
Exclusion Criteria:
* Use of any fibre supplementation (within the last month before screening or ongoing)
* Use of antibiotics in the lasts …
Inclusion Criteria:
* A diagnosis of type 1 diabetes, as made by their primary clinician
* A time in range of \<80% in the last four weeks before screening
Exclusion Criteria:
* Use of any fibre supplementation (within the last month before screening or ongoing)
* Use of antibiotics in the lasts three months before screening or during study period
* Active infection during the study visit
* Inability or unwillingness to donate feces or urine.
* Illicit drug use (e.g. MDMA/amphetamine/cocaine/heroin/GHB) in the past three months or use during the study period.
* Inability or unwillingness to provide informed consent.
* Absence of a large bowel (ie colostomy)
* Active inflammatory bowel disease
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