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In-hospital Diabetes Management With Flash Glucose Monitoring (isCGM) - the INDIGO Study, Part A 13

Beëindigd
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De klinische studie NCT04650945 is een interventioneel studie bij Type 1 diabetes mellitus, Type 2 diabetes mellitus, Diabetes mellitus met de status beëindigd. Het doel is om 13 deelnemers te includeren vanaf 4 januari 2021. De studie wordt geleid door de Universiteit van Aarhus en de voltooiing is gepland op 16 november 2022. Laatste update op ClinicalTrials.gov: 21 november 2022.
Beknopte samenvatting
The aim of the study is to investigate the applicability of a Flash glucose monitoring sensor (Freestyle Libre, isCGM) for in-hospital glucose monitoring in patients with diabetes requiring nutritional therapy (tube feeding or parenteral feeding).
Uitgebreide beschrijving
All patients who meet study criteria will be invited to participate in the study. All patients included in the study will be followed by a trained clinical diabetes specialist and a trained study nurse (study personnel) for glucose management during their hospitalization. All patients included in the study will receive a Freestyle Libre isCGM. The patients will be randomized to control (blinded isCGM glucose values t...Toon meer
Officiële titel

In-hospital Diabetes Management With Flash Glucose Monitoring (isCGM) - the INDIGO Study, Part A

Aandoeningen
Type 1 diabetes mellitusType 2 diabetes mellitusDiabetes mellitus
Andere studie-ID's
  • 1-10-72-188-20
NCT-ID
Startdatum (Werkelijk)
2021-01-04
Laatste update geplaatst
2022-11-21
Verwachte einddatum
2022-11-16
Inschrijving (Geschat)
13
Studietype
Interventioneel
FASE
N.v.t.
Status
Beëindigd
Trefwoorden
Continuous glucose monitoring
Hospitalization
Nutritional therapy
Primaire doel
Overige
Toewijzing
Gerandomiseerd
Interventiemodel
Parallel
Blindering
Enkelblind
Armen / Interventies
Deelnemersgroep/StudiearmInterventie/Behandeling
Actieve comparatorisCGM-arm
isCGM (intermittently scanned continuous glucose monitor) data obtained from a FreeStyle Libre Flash continuous glucose monitoring system will be viewed real-time and used to adjust diabetes treatment
isCGM group
As previously described
Geen interventiePOC-arm
POC glucose readings are used to adjust diabetes treatment. CGM data from the Freestyle Libre monitor are blinded to all and only gathered for comparison purposes to intervention group.
N.v.t.
Primaire uitkomst
UitkomstmaatBeschrijving van de uitkomstmaatTijdsbestek
Glucose time in range (3,9-10 mmol/l) (% pr day)
Glucose time in range (3,9-10 mmol/l) when diabetes treatment is adjusted using isCGM compared with standard care using POC plasma glucose monitoring (PG) (% pr day)
2-14 days
Secundaire uitkomst
UitkomstmaatBeschrijving van de uitkomstmaatTijdsbestek
Mean glucose (mmol/l) isCGM versus POC PG
Mean glucose (mmol/l) when diabetes treatment is adjusted using isCGM compared with standard care using POC plasma glucose monitoring (PG)
2-14 days
Glycemic variability; coefficient of variation (CV) (in %)
CV when diabetes treatment is adjusted using isCGM compared with standard care using POC plasma glucose monitoring (PG)
2-14 days
Glycemic variability; standard deviation (SD)
SD when diabetes treatment is adjusted using isCGM compared with standard care using POC plasma glucose monitoring (PG)
2-14 days
Time in hypoglycemia (<3 mmol/L) (%)
Time in hypoglycemia (%) when diabetes treatment is adjusted using isCGM compared with standard care using POC plasma glucose monitoring (PG)
2-14 days
Time in hypoglycemia (<3,9 mmol/l) (%)
Time in hypoglycemia (%) when diabetes treatment is adjusted using isCGM compared with standard care using POC plasma glucose monitoring (PG)
2-14 days
Number of events with hypoglycemia (<3,9 mmol/l) (%)
Number of events with hypoglycemia per day (\<3,9 mmol/L for \>15 minutes) when diabetes treatment is adjusted using isCGM compared with standard care using POC plasma glucose monitoring (PG)
2-14 days
Time in hyperglycemia (>10 mmol/l) (%)
Time in hyperglycemia when diabetes treatment is adjusted using isCGM compared with standard care using POC plasma glucose monitoring (PG)
2-14 days
Glucose out of range: Time in hypoglycemia and time in hyperglycemia (<3,9 and >10 mmol/l) (%)
Glucose out of range: Time in hypoglycemia and time in hyperglycemia (\<3,9 and \>10 mmol/l) (%) when diabetes treatment is adjusted using isCGM compared with standard care using POC plasma glucose monitoring (PG)
2-14 days
Daily total insulin dosage (IE)
Daily total insulin dosage (IE) when diabetes treatment is adjusted using isCGM compared with standard care using POC plasma glucose monitoring (PG)
2-14 days
Time with active isCGM
Time with active isCGM (%) in intervention group
2-14 days
Geschiktheidscriteria

Leeftijd van deelnemers
Volwassene, Oudere volwassene
Minimumleeftijd
18 Years
Geslachten die in aanmerking komen voor de studie
Allen
  • Expected length of hospital stay of at least 48 hours
  • Diagnosed with diabetes
  • Literate in Danish
  • Nutritional therapy using tube feeding or parenteral nutritional therapy
  • Admission to Department of Gastrointestinal Surgery or Department of Heart-, Lung-, and Vascular surgery, both at Aarhus University Hospital, Denmark.

  • Pregnancy
  • Patient unable to provide informed consent
  • Patient unable to use mobile phone for reading isCGM sensor
  • Known allergy to adhesives
  • Anticipated MRI during the hospital admission
  • Patients using CGM prior to hospital admission
Aarhus University Hospital logoAarhus University Hospital
Verantwoordelijke instantie
Julie Støy, Hoofdonderzoeker, Principal investigator, University of Aarhus
Geen contactgegevens beschikbaar
1 Studielocaties in 1 landen
Aarhus university hospital, Aarhus, 8200, Denmark