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Die klinische Studie NCT06628453 (CGM2) für Typ-2-Diabetes mellitus (T2DM), Schwangerschaft ist offene rekrutierung. In der Kartenansicht des Klinische Studien Radar und den KI-Entdeckungstools finden Sie alle Details. Oder stellen Sie hier Ihre Fragen. | ||
Eine Studie entspricht den Filterkriterien
Kartenansicht
CGM for Management of Type 2 Diabetes in Pregnancy (CGM2) 564
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 NCT06628453 (CGM2) ist eine interventionsstudie zur Untersuchung von Typ-2-Diabetes mellitus (T2DM), Schwangerschaft und hat den Status offene rekrutierung. Die Studie startete am 8. April 2025 und soll 564 Teilnehmer aufnehmen. Durchgeführt von Universität von Alabama in Birmingham ist der Abschluss für 1. Juli 2029 geplant. Die Daten von ClinicalTrials.gov wurden zuletzt am 15. Juni 2025 aktualisiert.
Kurzbeschreibung
The goal of this clinical trial is to learn if continuous glucose monitoring works better than self-monitoring of blood glucose (fingersticks) to treat type 2 diabetes in pregnancy. It will also learn about all risk factors (biologic, personal, social) for maternal and infant complications in type 2 diabetes pregnancies. The main questions it aims to answer are:
- Does continuous glucose monitoring improve infant o...
Ausführliche Beschreibung
We will conduct a multicenter, open-label randomized controlled trial of pregnant individuals with T2DM to test the effectiveness of CGM at improving maternal and neonatal outcomes, compared to SMBG. All pregnant women who have T2DM will be screened for eligibility. If a patient is eligible, the study will be explained to them and if they consent to participate, they will be randomized centrally in a 1:1 ratio to CGM...Mehr anzeigen
Offizieller Titel
Continuous Glucose Monitoring for Management of Type 2 Diabetes in Pregnancy
Erkrankungen
Typ-2-Diabetes mellitus (T2DM)SchwangerschaftPublikationen
Wissenschaftliche Artikel und Forschungspapiere zu dieser klinischen Studie:Weitere Studien-IDs
- CGM2
- IRB-300013640
- 1R01HD113612 (Zuwendung/Vertrag der US-NIH)
NCT-Nummer
Studienbeginn (tatsächlich)
2025-04-08
Zuletzt aktualisiert
2025-06-15
Studienende (vorauss.)
2029-07
Geplante Rekrutierung
564
Studientyp
Interventionsstudie
PHASE
Nicht zutreffend
Status
Offene Rekrutierung
Stichwörter
Diabetes
Pregnancy
CGM
Pregnancy
CGM
Primäres Ziel
Behandlung
Zuteilungsmethode
Randomisiert
Interventionsmodell
Parallel
Verblindung
Keine (offene Studie)
Studienarme/Interventionen
| Teilnehmergruppe/Studienarm | Intervention/Behandlung |
|---|---|
ExperimentellContinuous Glucose Monitoring Real-time continuous glucose monitoring | CGM Real-time continuous glucose monitoring |
Keine InterventionSelf-Monitoring of Blood Glucose Self-monitoring of blood glucose (standard of care) | Nicht zutreffend |
Hauptergebnismessungen
Nebenergebnismessungen
| Ergebnismessung | Beschreibung der Messung | Zeitrahmen |
|---|---|---|
Time in Range (TIR) at 34 weeks gestation | Percentage of time spent within target range (63-140mg/dL) on Continuous Glucose Monitoring at 34 weeks gestation | 33 to 35 weeks gestation |
Composite Neonatal Morbidity | Composite morbidity of the neonate including one or more of preterm birth (delivery less than 37 weeks for any indication), birth trauma (shoulder dystocia with nerve injury, clavicular or humeral fracture or 3 or more maneuvers to resolve), hypoglycemia (requiring treatment with dextrose gel or IV within 24 hours of birth), hyperbilirubinemia (requiring phototherapy within 72 hours of birth), large-for-gestational-age infant (birthweight greater than the 90th percentile for gestational age), and miscarriage, stillbirth or neonatal death prior to hospital discharge. | From the date of delivery to the date of neonatal hospital discharge, assessed up to 12 months of life |
| Ergebnismessung | Beschreibung der Messung | Zeitrahmen |
|---|---|---|
Preterm birth | Delivery less than 37 weeks gestation | Delivery |
Birth trauma | Shoulder dystocia with nerve injury, clavicular or humeral fracture or 3 or more maneuvers to relieve | Delivery |
Neonatal hypoglycemia | Low neonatal glucose requiring treatment with dextrose gel or IV within 24 hours of life | Delivery to 24 hours of life |
Hyperbilirubinemia | Elevated bilirubin requiring phototherapy within 72 hours of life | Delivery to 72 hours of life |
Large-for-gestational-age (LGA) neonate | Birthweight greater than the 90th percentile for gestational age | Delivery |
Small-for-gestational-age (SGA) neonate | Birthweight less than the 10th percentile for gestational age | Delivery |
Fetal glucose | Concentration of umbilical cord blood glucose (mg/dL) | Delivery |
Fetal insulin | Concentration of umbilical cord blood insulin (uU/mL) | Delivery |
Fetal C-peptide | Concentration of umbilical cord blood C-peptide (ng/mL) | Delivery |
Fetal leptin | Concentration of umbilical cord blood leptin (ng/mL) | Delivery |
Fetal ghrelin | Concentration of umbilical cord blood ghrelin (uU/L) | Delivery |
Fetal surfactant protein D | Concentration of umbilical cord blood surfactant protein D (ng/mL) | Delivery |
Time Above Range (TAR) at 34 weeks | Percentage of time spent above range greater than 140mg/dL on Continuous Glucose Monitoring (CGM) at 34 weeks | 33 to 35 weeks |
Time Below Range (TBR) at 34 weeks | Percentage of time spent below range less than 63mg/dL on Continuous Glucose Monitoring at 34 weeks | 33 to 35 weeks |
Mean glucose at 34 weeks | Average glucose in mg/dL using Continuous Glucose Monitoring data at 34 weeks | 33 to 35 weeks |
Glucose Management Indicator (GMI) | Glucose management indicator as an estimate of hemoglobin A1c calculated using mean glucose on CGM at 34 weeks | 33 to 35 weeks |
Glucose variability at 34 weeks | Coefficient of variation calculated as the mean glucose divided by standard deviation using Continuous Glucose Monitoring data at 34 weeks | 33 to 35 weeks |
Mean fasting glucose at 34 weeks | Average glucose at 6-7am on Continuous Glucose Monitoring at 34 weeks | 33 to 35 weeks |
Hemoglobin A1c at Delivery | Hemoglobin A1c (%) at delivery | Delivery |
Insulin total daily dose at delivery | Total number of units of insulin taken per day at time of delivery | Delivery |
Cesarean delivery | First cesarean delivery or cesarean delivery after a history of prior cesarean | Delivery |
Glucose Monitoring Satisfaction | Score on glucose monitoring satisfaction survey at delivery | Delivery |
Fetal or neonatal death | Miscarriage (pregnancy loss less than 20 weeks), stillbirth (fetal death at 20 weeks or more), or neonatal death (death after birth up to 28 days of life) | From the date of randomization to the date of neonatal hospital discharge, assessed up to 12 months of life |
Neonatal Intensive Care Unit (NICU) Admission | Admission to the neonatal intensive care unit with length of stay greater than 24 hours | From the date of delivery to the date of neonatal hospital discharge, assessed up to 12 months of life |
Neonatal length of stay | Duration of neonatal hospitalization after delivery | From the date of delivery to the date of neonatal hospital discharge, assessed up to 12 months of life |
Neonatal mechanical ventilation | Neonate requiring intubation and mechanical ventilation for respiratory support | From the date of delivery to the date of neonatal hospital discharge, assessed up to 12 months of life |
Insulin increase during pregnancy | Percentage change in total daily dose of insulin at delivery compared to enrollment | From the date of randomization to the date of delivery, assessed up to 9 months |
Preeclampsia | Elevated blood pressure greater than 140/90 mmHg after 20 weeks gestation with proteinuria or other severe features by ACOG criteria (may be superimposed on chronic hypertension or not) | From the date of randomization to the date of maternal hospital discharge after delivery, assessed up to 9 months |
Postpartum infection | Developing one or more of endometritis, wound infection or other wound complication such as seroma, hematoma or dehiscence) | From the date of delivery through 6 weeks' postpartum |
Glucose Monitoring Adherence | Defined as percentage of expected self-monitoring of blood glucose (SMBG) values completed based on recommended 4 values per day for participants in the SMBG arm and percentage of time Continuous Glucose Monitoring (CGM) in use in the CGM arm | From the date of randomization to the date of delivery, assessed up to 9 months |
Teilnahme-Assistent
Eignungskriterien
Zugelassene Altersgruppen
Erwachsene
Mindestalter
18 Years
Zugelassene Geschlechter
Weiblich
- Type 2 diabetes mellitus treated with daily insulin injections or oral hypoglycemic agents diagnosed before pregnancy or at less than 14 weeks gestation with hemoglobin A1c 6.5% or greater
- Pregnant with viable fetus at 6 to less than 23 weeks gestation
- Maternal age 18-50 years old
- Unable or unwilling to wear CGM due to intolerance to medical-grade adhesives or skin conditions
- Multiple gestation
- Major fetal anomaly or two or more minor fetal anomalies
- Planned delivery outside study consortium
- Participating in another conflicting interventional study
- Participation in this trial in a previous pregnancy
- Patient unable to consent
- Physician refusal for other reasons
National Institutes of Health (NIH)
Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
Verantwortliche Partei
Ashley N. Battarbee, Hauptprüfer, Associate Professor, University of Alabama at Birmingham
Zentrale Studienkontakte
Kontakt: Ashley Battarbee, MD, MSCR, 205-975-2361, [email protected]
7 Studienstandorte in 1 Ländern
Alabama
University of Alabama at Birmingham, Birmingham, Alabama, 35233, United States
Ashley Battarbee, Kontakt, 205-975-2361, [email protected]
Offene Rekrutierung
California
University of California at San Diego, San Diego, California, 92121, United States
Gladys Ramos, MD, Kontakt, 858-657-7200, [email protected]
Offene Rekrutierung
North Carolina
University of North Carolina - Chapel Hill, Chapel Hill, North Carolina, 27599, United States
Kim Boggess, MD, Kontakt, 919-966-2131, [email protected]
Offene Rekrutierung
Oregon
Oregon Health and Science University, Portland, Oregon, 97213, United States
Amy Valent, DO, MCR, Kontakt, 503-418-4200, [email protected]
Offene Rekrutierung
Pennsylvania
University of Pennsylvania, Philadelphia, Pennsylvania, 19104, United States
Celeste Durnwald, MD, Kontakt, 800-789-7366, [email protected]
Offene Rekrutierung
South Carolina
Prisma Health Greenville Memorial Hospital, Greenville, South Carolina, 29605, United States
Daniel Pasko, MD, Kontakt, 864-455-7000, [email protected]
Offene Rekrutierung
Texas
University of Texas Health Science Center at Houston, Houston, Texas, 77030, United States
Michal Fishel Bartal, MD, Kontakt, 832-325-7133, [email protected]
Offene Rekrutierung