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Evaluating Glucose Control Using a Next-Generation AID Algorithm in Individuals With T1D (EVOLUTIONT1D)

4. September 2026 aktualisiert von: Insulet Corporation

Evaluation Glucose Control Using a Next-Generation Automated Insulin Delivery Algorithm in Individuals With Type 1 Diabetes: EVOLUTION T1D

Feasibility study to evaluate the safety and feasibility of Omnipod automated insulin delivery algorithms in individuals with type 1 diabetes. This study will enroll up to 80 participants to have a minimum of 48 participants to initiate the use of Omnipod. The study will include hotel and outpatient evaluation periods.

Studienübersicht

Studientyp

Interventionell

Einschreibung (Geschätzt)

80

Phase

  • Unzutreffend

Kontakte und Standorte

Dieser Abschnitt enthält die Kontaktdaten derjenigen, die die Studie durchführen, und Informationen darüber, wo diese Studie durchgeführt wird.

Studienkontakt

Studieren Sie die Kontaktsicherung

Studienorte

      • Christchurch, Neuseeland, 8140
        • Rekrutierung
        • University of Otago
        • Hauptermittler:
          • Martin deBock, FRACP, PHD
        • Kontakt:

Teilnahmekriterien

Forscher suchen nach Personen, die einer bestimmten Beschreibung entsprechen, die als Auswahlkriterien bezeichnet werden. Einige Beispiele für diese Kriterien sind der allgemeine Gesundheitszustand einer Person oder frühere Behandlungen.

Zulassungskriterien

Studienberechtigtes Alter

  • Kind
  • Erwachsene
  • Älterer Erwachsener

Akzeptiert gesunde Freiwillige

Ja

Beschreibung

Inclusion Criteria:

  • Age at time of consent 2-70 years (inclusive)
  • Type 1 diabetes diagnosis for at least 6 months, for those aged 8-70 years, or 3 months for those aged 2-7 years, based on Investigator assessment
  • Basal/Bolus insulin delivery via multiple daily injections or insulin pump with or without automation
  • Willing to use the following types of U-100 insulin during the study: Humalog U-100, Novorapid or their generic equivalents
  • Deemed appropriate for pump therapy per Investigator's assessment considering previous history of severe hypoglycemic and hyperglycemic events, and other comorbidities
  • If using noninsulin glucose-lowering medications or weight reduction medications, dose has been stable for 6-weeks prior to screening; and participant is willing to not change the dose unless required for safety purposes.
  • Investigator has confidence that the participant can safely operate all study devices and can adhere to the protocol
  • Willing to wear the system continuously throughout the study
  • Willing and able to sign the Informed Consent Form (ICF) or has a parent/guardian willing and able to sign the ICF. Assent will be obtained from participants per local regulatory requirements
  • Able to read and understand English
  • If of childbearing potential, willing and able to have pregnancy testing

Exclusion Criteria:

  • Any medical condition, which in the opinion of the Investigator, would put the participant at an unacceptable safety risk. This may include untreated malignancy, unstable cardiac disease, unstable or end-stage renal disease, unstable proliferative retinopathy, unstable psychiatric conditions such as eating disorders, drug or alcohol abuse.
  • Current or known history of coronary artery disease that is not stable with medical management, including unstable angina, or a history of myocardial infarction, percutaneous coronary intervention, coronary artery bypass grafting, or arrhythmias requiring intervention within the 12 months prior to screening
  • Any planned surgery during the study which could be considered major in the opinion of the Investigator
  • History of more than 1 severe hypoglycaemia in the past 6 months. Severe hypoglycaemia is defined as an event that requires the assistance of another person due to altered consciousness, and requires another person to actively administer carbohydrate, glucagon, or other resuscitative actions
  • History of more than 1 diabetic ketoacidosis (DKA) in the past 6 months, unrelated to an intercurrent illness; kinked, dislodged, or occluded cannula; or initial diabetes diagnosis Unable to tolerate adhesive tape or has any unresolved skin condition that could impact sensor or pump placement
  • Blood disorder or dyscrasia within 3 months prior to screening, which in the Investigator's opinion could interfere with determination of HbA1c
  • Use of hydroxyurea
  • Plans to receive blood transfusion over the course of the study
  • Has taken systemic corticosteroids (oral or injectable) within 4 weeks or has had a local steroid injection (intraarticular, epidural) within 1 week prior to screening or plans to take oral or injectable steroids during the study
  • Use of non-insulin glucose-lowering medication or weight loss medications other than metformin and/or GLP1, in the 4 weeks prior to screening. Participants taking metformin and/or GLP1 should remain on a steady dose without dose increases during study participation
  • Pregnant or lactating, or is of childbearing potential and not using an acceptable form of birth control (acceptable forms of contraception include abstinence, barrier methods such as condoms, hormonal contraceptives, intrauterine device, surgical sterilisation such as tubal ligation or hysterectomy, or vasectomised partner); childbearing potential means that menstruation has started, and the participant is not surgically sterile or greater than 12 months post-menopausal).
  • In the past 30-days, has participated in a clinical study using any investigational drug or any investigational device that in the opinion of the investigator may have therapeutic impact on their diabetes management. Additionally, may not intend to participate in any other interventional clinical study during this study period
  • Unable to follow clinical protocol for the duration of the study or is otherwise deemed unacceptable to participate in the study per the Investigator's clinical judgment
  • Participant is an employee of Insulet, an Investigator or a member of Investigator's study team, or immediate family member of any of the aforementioned

Studienplan

Dieser Abschnitt enthält Einzelheiten zum Studienplan, einschließlich des Studiendesigns und der Messung der Studieninhalte.

Wie ist die Studie aufgebaut?

Designdetails

  • Hauptzweck: Behandlung
  • Zuteilung: Nicht randomisiert
  • Interventionsmodell: Einzelgruppenzuweisung
  • Maskierung: Keine (Offenes Etikett)

Waffen und Interventionen

Teilnehmergruppe / Arm
Intervention / Behandlung
Experimental: Adults with T1D using Omnipod M
Participants will use the Omnipod M System
Experimental: Adults and pediatrics with T1D using Omnipod S
Participants will use the Omnipod S System

Was misst die Studie?

Primäre Ergebnismessungen

Ergebnis Maßnahme
Maßnahmenbeschreibung
Zeitfenster
Percentage of time <54 mg/dL
Zeitfenster: 72-hour Omnipod M Hotel Period
CGM percent time <54 mg/dL compared to standard therapy
72-hour Omnipod M Hotel Period
Percentage of time <70 mg/dL
Zeitfenster: 72-hour Omnipod M Hotel Period
CGM percent time <70 mg/dL compared to standard therapy
72-hour Omnipod M Hotel Period
Percentage of time >180 mg/dL
Zeitfenster: 72-hour Omnipod M Hotel Period
CGM percent time >180 mg/dL compared to standard therapy
72-hour Omnipod M Hotel Period
Percentage of time <54 mg/dL
Zeitfenster: 4-week Omnipod M outpatient
CGM percent time <54 mg/dL compared to standard therapy
4-week Omnipod M outpatient
Percentage of time <54 mg/dL
Zeitfenster: Final 3 weeks of Omnipod S outpatient
CGM percent time <54 mg/dL compared to initial data collection phase
Final 3 weeks of Omnipod S outpatient
Percentage of time <70 mg/dL
Zeitfenster: 4-week Omnipod M outpatient
CGM percent time <70 mg/dL compared to standard therapy
4-week Omnipod M outpatient
Percentage of time <70 mg/dL
Zeitfenster: Final 3-weeks Omnipod S outpatient
CGM percent time <70 mg/dL compared to initial data collection phase
Final 3-weeks Omnipod S outpatient
Percentage of time >180 mg/dL
Zeitfenster: 4-week Omnipod M outpatient
CGM percent time >180 mg/dL compared to standard therapy
4-week Omnipod M outpatient
Percentage of time >180 mg/dL
Zeitfenster: Final 3-weeks Omnipod S outpatient
CGM percent time >180 mg/dL compared to initial data collection phase
Final 3-weeks Omnipod S outpatient

Sekundäre Ergebnismessungen

Ergebnis Maßnahme
Maßnahmenbeschreibung
Zeitfenster
Incidence rate of severe hypoglycemia (SH)
Zeitfenster: 72-hour hotel period and 4-week outpatient period
events per person months
72-hour hotel period and 4-week outpatient period
Incidence rate of diabetic ketoacidosis (DKA)
Zeitfenster: 72-hour hotel period and 4-week outpatient period
events per person months
72-hour hotel period and 4-week outpatient period
Mean glucose
Zeitfenster: 4-weeks Omnipod M outpatient
Mean glucose compared to standard therapy
4-weeks Omnipod M outpatient
Mean glucose
Zeitfenster: Final 3-weeks Omnipod S outpatient
Mean glucose compared to initial data collection
Final 3-weeks Omnipod S outpatient
Percentage of time >250 mg/dL
Zeitfenster: 4-weeks Omnipod M outpatient
CGM percent time >250 mg/dL compared to baseline
4-weeks Omnipod M outpatient
Percentage of time >250 mg/dL
Zeitfenster: Final 3-weeks Omnipod S outpatient
CGM percent time >250 mg/dL compared to initial data collection
Final 3-weeks Omnipod S outpatient
Percentage of time >300 mg/dL
Zeitfenster: 4-weeks Omnipod M outpatient
CGM percent time >300 mg/dL compared to standard therapy
4-weeks Omnipod M outpatient
Percentage of time >300 mg/dL
Zeitfenster: Final 3-weeks Omnipod S outpatient
CGM percent time >300 mg/dL compared to initial data collection phase
Final 3-weeks Omnipod S outpatient
Percentage of time 70-180 mg/dL
Zeitfenster: 4-weeks Omnipod M outpatient
CGM percent time 70-180 mg/dL compared to standard therapy
4-weeks Omnipod M outpatient
Percentage of time 70-180 mg/dL
Zeitfenster: Final 3-weeks Omnipod S outpatient
CGM percent time 70-180 mg/dL compared to initial data collection
Final 3-weeks Omnipod S outpatient
Standard Deviation
Zeitfenster: 4-weeks Omnipod M outpatient
Standard deviation compared to standard therapy
4-weeks Omnipod M outpatient
Standard Deviation
Zeitfenster: Final 3-weeks Omnipod S outpatient
Standard deviation compared to initial data collection
Final 3-weeks Omnipod S outpatient
Coefficient of variation
Zeitfenster: 4-weeks Omnipod M outpatient
Coefficient of variation compared to standard therapy
4-weeks Omnipod M outpatient
Coefficient of variation
Zeitfenster: Final 3-weeks Omnipod S outpatient
Coefficient of variation compared to standard therapy
Final 3-weeks Omnipod S outpatient
Average total daily insulin (TDI)
Zeitfenster: 4-weeks Omnipod M outpatient
Average TDI compared to standard therapy
4-weeks Omnipod M outpatient
Average total daily insulin (TDI)
Zeitfenster: Final 3-weeks Omnipod S outpatient
Average TDI compared to initial data collection
Final 3-weeks Omnipod S outpatient
Average TDI/kg
Zeitfenster: 4-weeks Omnipod M outpatient
Average TDI/kg compared to standard therapy
4-weeks Omnipod M outpatient
Average TDI/kg
Zeitfenster: Final 3-weeks Omnipod S outpatient
Average TDI/kg compared to initial data collection
Final 3-weeks Omnipod S outpatient
Post-prandial glycemic metrics
Zeitfenster: Up to 4-hours following tracked meal
Descriptive statistics for CGM metrics during and following meals will be calculated for Omnipod M (hotel) and Omnipod S (outpatient)
Up to 4-hours following tracked meal
Post-exercise session glycemic metrics
Zeitfenster: Up to 2-hours following exercise
Descriptive statistics for CGM metrics during and following exercise will be calculated for Omnipod M (hotel) and Omnipod S (outpatient)
Up to 2-hours following exercise
Incidence rate of severe hypoglycemia (SH)
Zeitfenster: Final 3-weeks Omnipod S outpatient
events per person months
Final 3-weeks Omnipod S outpatient
Incidence rate of diabetic ketoacidosis (DKA)
Zeitfenster: Final 3-weeks Omnipod S outpatient
events per person months
Final 3-weeks Omnipod S outpatient

Mitarbeiter und Ermittler

Hier finden Sie Personen und Organisationen, die an dieser Studie beteiligt sind.

Studienaufzeichnungsdaten

Diese Daten verfolgen den Fortschritt der Übermittlung von Studienaufzeichnungen und zusammenfassenden Ergebnissen an ClinicalTrials.gov. Studienaufzeichnungen und gemeldete Ergebnisse werden von der National Library of Medicine (NLM) überprüft, um sicherzustellen, dass sie bestimmten Qualitätskontrollstandards entsprechen, bevor sie auf der öffentlichen Website veröffentlicht werden.

Haupttermine studieren

Studienbeginn (Tatsächlich)

25. Mai 2026

Primärer Abschluss (Geschätzt)

31. Dezember 2026

Studienabschluss (Geschätzt)

1. Februar 2027

Studienanmeldedaten

Zuerst eingereicht

11. Mai 2026

Zuerst eingereicht, das die QC-Kriterien erfüllt hat

11. Mai 2026

Zuerst gepostet (Tatsächlich)

18. Mai 2026

Studienaufzeichnungsaktualisierungen

Letztes Update gepostet (Tatsächlich)

10. September 2026

Letztes eingereichtes Update, das die QC-Kriterien erfüllt

4. September 2026

Zuletzt verifiziert

1. September 2026

Mehr Informationen

Begriffe im Zusammenhang mit dieser Studie

Arzneimittel- und Geräteinformationen, Studienunterlagen

Studiert ein von der US-amerikanischen FDA reguliertes Arzneimittelprodukt

Nein

Studiert ein von der US-amerikanischen FDA reguliertes Geräteprodukt

Nein

Produkt, das in den USA hergestellt und aus den USA exportiert wird

Ja

Diese Informationen wurden ohne Änderungen direkt von der Website clinicaltrials.gov abgerufen. Wenn Sie Ihre Studiendaten ändern, entfernen oder aktualisieren möchten, wenden Sie sich bitte an register@clinicaltrials.gov. Sobald eine Änderung auf clinicaltrials.gov implementiert wird, wird diese automatisch auch auf unserer Website aktualisiert .

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