- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT04620967
Fast-Acting Insulin Aspart and Insulin Pump Settings
12. februar 2021 opdateret af: Kirsten Nørgaard
Fast-Acting Insulin Aspart and Insulin Pump Settings: THE FAST PUMP SETTING STUDY
To clarify the role of fast-acting insulin aspart (Fiasp) in insulin pump-treated type 1 diabetes more research is needed.
The aim of this study is twofold:
- to compare the effects of Fiasp and Iasp in adults with type 1 diabetes who are using insulin pump and CGM and who are attending a diabetes out-patient clinic with extensive expertise in insulin pump and CGM therapy.
- to determine differences in insulin pump settings when insulin pumps are optimally adjusted to each of the two insulin types.
Studieoversigt
Status
Ukendt
Betingelser
Intervention / Behandling
Undersøgelsestype
Interventionel
Tilmelding (Forventet)
40
Fase
- Fase 4
Kontakter og lokationer
Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.
Studiekontakt
- Navn: Signe Schmidt, MD PhD
- Telefonnummer: +45 51174785
- E-mail: signe.schmidt@regionh.dk
Studiesteder
-
-
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Gentofte, Danmark, 2820
- Rekruttering
- Steno Diabetes Center Copenhagen
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Kontakt:
- Signe Schmidt, MD PhD
- Telefonnummer: +45 51174785
- E-mail: signe.schmidt@regionh.dk
-
Underforsker:
- Ajenthen Ranjan, MD PhD
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Underforsker:
- Hanne-Charlotte Andersen, RN
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Underforsker:
- Signe Schmidt, MD PhD
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-
Deltagelseskriterier
Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.
Berettigelseskriterier
Aldre berettiget til at studere
18 år og ældre (Voksen, Ældre voksen)
Tager imod sunde frivillige
Ingen
Køn, der er berettiget til at studere
Alle
Beskrivelse
Inclusion Criteria:
- Type 1 diabetes for ≥ 5 years
- HbA1c 53-75 mmol/mol (7.0-9.0%)
- Insulin pump treatment for ≥ 6 months (all insulin pump makes except hybrid closed-loop systems are eligible for inclusion)
- CGM use for ≥ 6 months (all CGM makes are eligible for inclusion)
- Carbohydrate counting for all snacks and meals
- Use of the insulin pump bolus calculator for all meals and snacks
Exclusion Criteria:
- Breast-feeding, pregnant, planning to become pregnant or of child-bearing potential and not using adequate contraceptive methods
- Gastroparesis (clinical assessment)
- Shift work
- Changing insulin needs throughout the menstrual cycle that requires different basal rate patterns
- Use of a hybrid closed-loop system
- Use of flash glucose monitoring
- Use of anti-diabetic medicine (other than insulin), corticosteroids or other drugs affecting glucose metabolism during the study period or within 30 days prior to study start
- Chronic paracetamol use
- Alcohol or drug abuse
- Severe cardiac disease or retinopathy contraindicating HbA1c below 53 mmol/mol
- Impaired renal function (eGFR< 60 ml/min/1.73 m2)
- History of local skin reactions to Fiasp and/or Iasp
- Other concomitant medical or psychological condition that according to the investigator's assessment makes the patient unsuitable for study participation
- Lack of compliance with key study procedures at the discretion of the investigator
- Unacceptable adverse events at the discretion of the investigator
- Less than 40 weeks guarantee remaining on insulin pump
Studieplan
Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Behandling
- Tildeling: Randomiseret
- Interventionel model: Crossover opgave
- Maskning: Tredobbelt
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
---|---|
Eksperimentel: Iasp-Fiasp
First period: Insulin pump with Iasp Second period: Insulin pump with Fiasp
|
Insulin aspart (Iasp) in insulin pump
Fast-acting insulin aspart (Fiasp) in insulin pump
|
Eksperimentel: Fiasp-Iasp
First period: Insulin pump with Fiasp Second period: Insulin pump with Iasp
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Insulin aspart (Iasp) in insulin pump
Fast-acting insulin aspart (Fiasp) in insulin pump
|
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
---|---|---|
Time in range
Tidsramme: Last two weeks of the 16-week interventions
|
Difference in time spent with glucose values in the range 3.9-10.0
mmol/l between Fiasp and Iasp treatment assessed by continuous glucose monitoring
|
Last two weeks of the 16-week interventions
|
Sekundære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
---|---|---|
Mean glucose
Tidsramme: Last two weeks of the 16-week interventions
|
Difference in mean glucose between Fiasp and Iasp treatment assessed by continuous glucose monitoring
|
Last two weeks of the 16-week interventions
|
Coefficient of variation
Tidsramme: Last two weeks of the 16-week interventions
|
Difference in coefficient of variation between Fiasp and Iasp treatment assessed by continuous glucose monitoring
|
Last two weeks of the 16-week interventions
|
Time below range level 1
Tidsramme: Last two weeks of the 16-week interventions
|
Difference in time spent with glucose values below 3.9 mmol/l between Fiasp and Iasp treatment assessed by continuous glucose monitoring
|
Last two weeks of the 16-week interventions
|
Time below range level 2
Tidsramme: Last two weeks of the 16-week interventions
|
Difference in time spent with glucose values below 3.0 mmol/l between Fiasp and Iasp treatment assessed by continuous glucose monitoring
|
Last two weeks of the 16-week interventions
|
Time above range level 1
Tidsramme: Last two weeks of the 16-week interventions
|
Difference in time spent with glucose values above 10.0 mmol/l between Fiasp and Iasp treatment assessed by continuous glucose monitoring
|
Last two weeks of the 16-week interventions
|
Time above range level 2
Tidsramme: Last two weeks of the 16-week interventions
|
Difference in time spent with glucose values above 13.9 mmol/l between Fiasp and Iasp treatment assessed by continuous glucose monitoring
|
Last two weeks of the 16-week interventions
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Fructosamine
Tidsramme: 16 weeks
|
Difference in change in fructosamine between Fiasp and Iasp treatment
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16 weeks
|
Total daily insulin dose
Tidsramme: Last two weeks of the 16-week interventions
|
Difference between Fiasp and Iasp treatment in total daily insulin dose
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Last two weeks of the 16-week interventions
|
Total daily basal insulin dose
Tidsramme: Last two weeks of the 16-week interventions
|
Difference between Fiasp and Iasp treatment in total daily basal insulin dose
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Last two weeks of the 16-week interventions
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Total daily bolus insulin dose
Tidsramme: Last two weeks of the 16-week interventions
|
Difference between Fiasp and Iasp treatment in total daily bolus insulin dose
|
Last two weeks of the 16-week interventions
|
Severe hypoglycemia
Tidsramme: 16 weeks
|
Difference between Fiasp and Iasp treatment in number of severe hypoglycemia events
|
16 weeks
|
Ketoacidosis
Tidsramme: 16 weeks
|
Difference between Fiasp and Iasp treatment in number of ketoacidosis events
|
16 weeks
|
Samarbejdspartnere og efterforskere
Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.
Sponsor
Efterforskere
- Ledende efterforsker: Kirsten Nørgaard, MD DMSc, Steno Diabetes Center Copenhagen
Datoer for undersøgelser
Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.
Studer store datoer
Studiestart (Faktiske)
1. februar 2021
Primær færdiggørelse (Forventet)
30. juni 2022
Studieafslutning (Forventet)
30. juni 2022
Datoer for studieregistrering
Først indsendt
3. november 2020
Først indsendt, der opfyldte QC-kriterier
3. november 2020
Først opslået (Faktiske)
9. november 2020
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
16. februar 2021
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
12. februar 2021
Sidst verificeret
1. februar 2021
Mere information
Begreber relateret til denne undersøgelse
Nøgleord
Yderligere relevante MeSH-vilkår
- Glukosemetabolismeforstyrrelser
- Metaboliske sygdomme
- Sygdomme i immunsystemet
- Autoimmune sygdomme
- Sygdomme i det endokrine system
- Diabetes mellitus
- Diabetes mellitus, type 1
- Hypoglykæmiske midler
- Lægemidlers fysiologiske virkninger
- Insulin
- Insulin, Globin Zink
- Insulin Aspart
- Insulin, langtidsvirkende
- Insulin degludec, insulin aspart lægemiddelkombination
Andre undersøgelses-id-numre
- 2020-001158-23
- H-20022359 (Anden identifikator: Scientific Ethical Committee of the Capital Region of Denmark)
Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter
Studerer et amerikansk FDA-reguleret lægemiddelprodukt
Ingen
Studerer et amerikansk FDA-reguleret enhedsprodukt
Ingen
Disse oplysninger blev hentet direkte fra webstedet clinicaltrials.gov uden ændringer. Hvis du har nogen anmodninger om at ændre, fjerne eller opdatere dine undersøgelsesoplysninger, bedes du kontakte register@clinicaltrials.gov. Så snart en ændring er implementeret på clinicaltrials.gov, vil denne også blive opdateret automatisk på vores hjemmeside .
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