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Effectiveness and Safety Study of the Dexcom G4™ Continuous Glucose Monitoring System 72

Abgeschlossen
Die Details der klinischen Studie sind hauptsächlich auf Englisch verfügbar. Trial Radar KI kann jedoch helfen! Klicken Sie einfach auf 'Studie erklären', um die Informationen zur Studie in der ausgewählten Sprache anzuzeigen und zu besprechen.
Die klinische Studie NCT01514292 untersuchte Diabetes als interventionsstudie und hat den Status abgeschlossen. Die Studie begann am 1. Dezember 2011 mit 72 Teilnehmern. Sie wurde durchgeführt von DexCom, Inc. und am 1. Februar 2012 abgeschlossen. Die Daten von ClinicalTrials.gov wurden zuletzt am 5. Oktober 2015 aktualisiert.
Kurzbeschreibung
The purpose of this study is to evaluate the effectiveness and safety of the Dexcom G4 System when used as an adjuvant to blood glucose testing over a 7-day period in people >18 years-old with diabetes mellitus.

The primary objective is to characterize the System performance with respect to laboratory reference venous sample measurements. The device performance will be primarily evaluated in terms of point and rate...

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Ausführliche Beschreibung
The primary objective is to characterize the System performance with respect to laboratory reference venous sample measurements. The device performance will be primarily evaluated in terms of point and rate accuracy of the G4 System in reference to YSI. The trend accuracy of the device performance, i.e., continuous glucose error grid analysis, will be evaluated as well as the temporal G4 System accuracy at different ...Mehr anzeigen
Offizieller Titel

PTL-900590 Effectiveness and Safety Study of the Dexcom G4™ Continuous Glucose Monitoring System

Erkrankungen
Diabetes
Weitere Studien-IDs
  • PTL-900590
NCT-Nummer
NCT01514292
Studienbeginn (tatsächlich)
2011-12
Zuletzt aktualisiert
2015-10-05
Studienende (vorauss.)
2012-02
Geplante Rekrutierung
72
Studientyp
Interventionsstudie
PHASE
Nicht zutreffend
Status
Abgeschlossen
Primäres Ziel
Behandlung
Zuteilungsmethode
Nicht zutreffend
Interventionsmodell
Einarmige Studie
Verblindung
Keine (offene Studie)
Studienarme/Interventionen
Teilnehmergruppe/StudienarmIntervention/Behandlung
ExperimentellReal Time Continuous Glucose Monitoring System
7 day use of real time continuous glucose monitoring system
Continuous Glucose Monitoring of glucose levels (Dexcom)
Manipulation of glucose levels during multiple clinic days. Achieved through diet, exercise and insulin regimen defined in protocol.Evaluation of CGM performance characteristics in reference to a laboratory standard.
Hauptergebnismessungen
ErgebnismessungBeschreibung der MessungZeitrahmen
CGM Relative Differences to Laboratory Reference
The outcome measure is measured as the relative differences (%) of the CGM glucose value in reference to a laboratory reference, yellow spring instrument( YSI) glucose measurements.
7 days
Eignungskriterien

Zugelassene Altersgruppen
Erwachsene, Ältere Erwachsene
Mindestalter
18 Years
Zugelassene Geschlechter
Alle

  • Age 18 years or older;

  • Diagnosed with diabetes mellitus;

  • Use one of the following for their diabetes management:

    • intensive insulin therapy (IIT) or
    • non-intensive insulin therapy (non-IIT)

  • Intensive-insulin using (IIT) subjects only - During each in-clinic session, willing to have their blood glucose levels manipulated into high and low glucose levels. Subjects not on IIT will only be observed during each in-clinic session.

  • For subjects that exercise routinely (at least 3 times per week), willing to exercise on each in-clinic session, if asked;

  • Willing to take a minimum of 7 fingersticks per day during home use days;

  • Willing to refrain from the use of acetaminophen during sensor wear period and the day prior to sensor insertion;

  • Have extensive skin changes/diseases that preclude wearing the required number of devices on normal skin (e.g., extensive psoriasis, recent burns or severe sunburn, extensive eczema, extensive scarring, extensive tattoos, dermatitis herpetiformis) at the proposed wear sites;
  • Have a known allergy to medical-grade adhesives;
  • Are pregnant as demonstrated by a positive pregnancy test within 72 hours of sensor insertion,
  • Are on dialysis;
  • Have a hematocrit that is less than 36% or greater than 55% at screening visit;
  • Currently participating in another investigational study protocol (if a subject has recently completed participation in another drug study, the subject must have completed that study at least 30 days prior to being enrolled in this study);
  • Have a history of cardiovascular disease (including, but not limited to ischemic heart disease, peripheral vascular disease, cardiomyopathy, cerebrovascular disease, congenital heart disease, or significant arrhythmias), epilepsy, severe migraines in the past 6 months, adrenal disease, syncope, significant hypoglycemia unawareness, or a history of severe hypoglycemia (requiring emergency medical intervention) within the last 6 months;
  • Have any chronic infectious disease or intercurrent illness that would interfere with their participation in the study or pose an excessive risk to study staff handling venous or capillary blood samples (e.g. HIV/AIDS, Hepatitis B or C);
  • Have a MRI scan, CT scan, or diathermy scheduled during the week of the study. If any of these procedures are required urgently during the study, subjects will notify the study staff, end their CGM session, and remove their sensor.
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4 Studienstandorte in 1 Ländern

California

Profil Institute for Clinical Research, Chula Vista, California, 91911, United States
AMCR Institute, Inc., Escondido, California, 92026, United States
Diablo Clinical Research, Walnut Creek, California, 94598, United States

Idaho

Rocky Mountain Diabetes and Osteoporosis Center, Idaho Falls, Idaho, 83404, United States