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Continuous Glucose Monitoring Parameter and Oral Glucose Tolerance Testing (OGTT) Parameters in Children and Young Adults With Cystic Fibrosis (CF)

NCT07930884, Not applicable, Recruiting, Northwell Health

Trial 10

As registered on ClinicalTrials.gov, in the graph's capture of the registry.

FieldValueSource
TitleContinuous Glucose Monitoring Parameter and Oral Glucose Tolerance Testing (OGTT) Parameters in Children and Young Adults With Cystic Fibrosis (CF)ClinicalTrials.gov
NCT numberNCT07930884ClinicalTrials.gov
StatusRecruitingClinicalTrials.gov
PhasesNot applicableClinicalTrials.gov
Enrollment30 participants, estimatedClinicalTrials.gov
Lead sponsorNorthwell HealthClinicalTrials.gov
ConditionsCystic Fibrosis Related Diabetes, CGMClinicalTrials.gov
InterventionsContinuous Glucose MonitorClinicalTrials.gov
First posted2026-11-12ClinicalTrials.gov
Last updated2026-11-12ClinicalTrials.gov

Registered outcomes 11

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescriptionSource
PrimaryAverage Blood Glucose Level from Continuous Glucose MonitoringUp to 10 days of CGM wear (within 3 months of the Oral Glucose Tolerance Test).Mean glucose level recorded over the continuous glucose monitoring (CGM) wear period (mg/dL)ClinicalTrials.gov
SecondaryPercentage of Time Glucose Exceeds 150 mg/dL from Continuous Glucose MonitoringUp to 10 days of CGM wear (within 3 months of the Oral Glucose Tolerance Test).The proportion of time during the CGM wear period that glucose levels were above 150 mg/dL (%)ClinicalTrials.gov
SecondaryPercentage of Time Glucose Exceeds 180 mg/dL from Continuous Glucose MonitoringUp to 10 days of CGM wear (within 3 months of the Oral Glucose Tolerance Test).The proportion of time during the CGM wear period that glucose levels were above 180 mg/dL (%)ClinicalTrials.gov
SecondaryFasting Plasma Glucose Level from Oral Glucose Tolerance TestSingle measurement at the start of the OGTT (within 3 months of CGM wear).Plasma glucose level measured after an overnight fast, as part of the Oral Glucose Tolerance Test (OGTT) (mg/dL)ClinicalTrials.gov
Secondary1 hour Plasma Glucose Level from Oral Glucose Tolerance TestSingle measurement 1 hour after glucose load (within 3 months of CGM wear).Plasma glucose level measured 1 hour after glucose administration as part of the Oral Glucose Tolerance Test (OGTT) (mg/dL)ClinicalTrials.gov
Secondary2-Hour Plasma Glucose Level from Oral Glucose Tolerance TestSingle measurement 2 hours after glucose load (within 3 months of CGM wear).Plasma glucose level measured 2 hours after glucose load administration during the OGTT (mg/dL)ClinicalTrials.gov
SecondaryForced Expiratory Volume in 1 Second (FEV1) as a Percentage of PredictedWithin 3 months of CGM placement (standard of care assessment).Lung function parameter reflecting the volume of air exhaled in the first second during a forced breath, expressed as a percentage of the predicted value. (%)ClinicalTrials.gov
SecondaryForced Vital Capacity (FVC) as a Percentage of PredictedWithin 3 months of CGM placement (standard of care assessment).Lung function parameter reflecting the total volume of air exhaled during a forced breath, expressed as a percentage of the predicted value (%)ClinicalTrials.gov
SecondaryHemoglobin A1c (HbA1c) LevelAt the time of OGTT (within 3 months of CGM wear).A measure of average blood glucose level (%)ClinicalTrials.gov
SecondaryBody Mass Index (BMI) Z-ScoreWithin 3 months of CGM placement (standard of care assessment).Age- and sex-adjusted Body Mass Index standardized score, reflecting nutritional status (z-score)ClinicalTrials.gov
SecondaryResponse to Survey Question on CFRD Screening PreferencesAfter 10 days of CGM wearParticipant's (and/or parent/guardian's) response to the Likert scale questions regarding preferences for Cystic Fibrosis Related DiabetesClinicalTrials.gov

Outcomes 0

Each outcome the trial posted results for, in ClinicalTrials.gov's words.

TypeOutcomeTime framePopulationUnitsMeasured asSource

Results by group 0

Each measurement the trial posted, group by group, in the words and numbers it posted.

OutcomeGroupCategoryValueSpreadUnitsSource

Participant flow 0

How many started, completed or left each group, period by period.

PeriodMilestoneGroupParticipantsUnits countedSource

Adverse events 0

Each adverse event the trial posted, group by group: the participants affected out of those at risk.

TypeEventOrgan systemGroupAffectedAt riskEventsSource

Adverse event totals 0

The totals the trial posted for each group.

TotalGroupAffectedAt riskSource

Papers 6

The papers the trial lists on ClinicalTrials.gov.

PMIDListed asSource
19605874BACKGROUNDPubMed
21115772BACKGROUNDPubMed
27268400BACKGROUNDPubMed
31036487BACKGROUNDPubMed
34537845BACKGROUNDPubMed
37274323BACKGROUNDPubMed

Trial comparisons 0

Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.

ComparisonSource

Tests 0

The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.

TestNamed asSource

Source 4

FieldValueSource
Releasetrials-2026-11-12-0.3.0ClinicalTrials.gov
Release manifest SHA-2564a570df2e7274cee2d4fa2959402fab41880e2cd412e4b590390035fbea69391ClinicalTrials.gov
Registry capture2026-11-12ClinicalTrials.gov
Results copy, AACT2026-03-23ClinicalTrials.gov

The same record as JSON

Release trials-2026-11-12-0.3.0

ClinicalTrials.gov's posted results, through CTTI's AACT: ClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299 ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

ClinicalTrials.gov: none stated ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.