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

2026년 11월 9일 업데이트: Northwell Health

As modulator therapies extend the lifespan of CF patients, the detection of complications like Cystic Fibrosis Related Diabetes (CFRD) becomes increasingly vital. The current gold standard for CFRD screening, the 2-hour OGTT, is cumbersome and suffers from low compliance. This study proposes that Continuous Glucose Monitoring (CGM) could offer a more comprehensive, easier, and potentially more compliant screening method. The research aims to correlate various CGM parameters (e.g., time in hyperglycemia) with traditional glycemic markers like OGTT glucose levels, GMI, average glucose, variability, and HbA1c. Additionally, the research seeks to understand patient and parent/guardian preferences for CFRD screening modalities. This prospective observational study will involve CF patients wearing a Dexcom CGM around the time of standard OGTT and HbA1c tests, followed by surveys, with the ultimate goal of paving the way for CGM to improve early detection and management of dysglycemia in CF children.

연구 개요

상태

모병

정황

개입 / 치료

상세 설명

As modulator therapy changes the landscape of cystic fibrosis (CF), children with CF will live longer and healthier lives with less pulmonary exacerbations. Still, other complications like Cystic Fibrosis Related Diabetes and underlying dysglycemia may become more apparent as lifespans of CF patients increase. It is therefore essential that clinicians have the tools to understand early stages of dysglycemia to prevent long term complications of CFRD. At present, 2 hours 75-gram OGTT remains the gold standard annual screen for CFRD. This test is both cumbersome for patients and limits a clinician's interpretation of glycemic control to a limited time frame. Although OGTT is currently used to diagnose CFRD, it can be cumbersome for patients and time consuming. OGTT compliance is therefore not surprisingly low in the CF population with about 49 % of CF centers having a more than 50% completion of annual OGTT. Continuous glucose monitoring (CGM), on the other hand, offers the ability to obtain more data on longer time periods in a much easier fashion. Thus, CGMs have the potential to glean a more fine-tuned understanding of a patient's glycemic control. Moreover, CGMs can make glycemic testing easier on patients, thereby increasing compliance of annual glycemic testing. The investigators hypothesize the correlation of CGM parameters of hyperglycemia like % of time > 180 mg/dl, % of time> 150 mg/dL with 1- and 2-hour OGTT glucose levels, Glucose Management Indicator (GMI), average glucose, glucose variability, and HbA1c levels. The investigators also aim to explore patient views and preferences of OGTT and CGM for screening of CFRD through surveys after CGM wear.

The investigators hope to be able to correlate 1- and 2-hour glucose values on OGTT to % in range parameters on a continuous glucose monitor. This will pave the way to better understand glycemic control in children with CF and risk for CFRD with data from a CGM even without an OGTT in the future. The investigators also hope to understand patient and parent/guardian preferences towards CFRD screening modalities.

Study Design: Prospective observational study. Eligible patients will have a CGM placed for up to10-day wear within the 3 months before or after clinically appropriate OGTT and A1c. OGTT testing will include 1- and 2-hour glucose levels and HbA1c as per standard of care. A Dexcom CGM will be placed in clinic onto the subjects upper arm. Survey exploring patient and parent/guardian preference will be provided after the CGM is removed.

연구 유형

중재적

등록 (추정된)

30

단계

  • 해당 없음

연락처 및 위치

이 섹션에서는 연구를 수행하는 사람들의 연락처 정보와 이 연구가 수행되는 장소에 대한 정보를 제공합니다.

연구 연락처

연구 장소

    • New York
      • New York, New York, 미국, 11042
        • 모병
        • Northwell Health
        • 연락하다:

참여기준

연구원은 적격성 기준이라는 특정 설명에 맞는 사람을 찾습니다. 이러한 기준의 몇 가지 예는 개인의 일반적인 건강 상태 또는 이전 치료입니다.

자격 기준

공부할 수 있는 나이

10년 (어린이, 성인)

건강한 자원 봉사자를 받아들입니다

아니

연구 대상 성별

모두

설명

Inclusion Criteria:

  1. Patients with Cystic Fibrosis
  2. 10-25 years of age who have obtained or will obtain a OGTT within 3 months of recruitment and CGM placement.

Exclusion Criteria:

  1. Diagnosis of diabetes mellitus type 1 or type 2
  2. Use of the following medication: steroid course, Metformin therapy,
  3. Concurrent CV disease or malignancy, kidney failure, lung transplant.
  4. Does not have access to personal Bluetooth device compatible with Dexcom G7 application.

공부 계획

이 섹션에서는 연구 설계 방법과 연구가 측정하는 내용을 포함하여 연구 계획에 대한 세부 정보를 제공합니다.

연구는 어떻게 설계됩니까?

디자인 세부사항

  • 주 목적: 상영
  • 할당: 해당 없음
  • 중재 모델: 단일 그룹 할당
  • 마스킹: 없음(오픈 라벨)

무기와 개입

참가자 그룹 / 팔
개입 / 치료
실험적: Pediatric Cystic Fibrosis Patients Undergoing Concurrent CGM Monitoring and OGTT Testing

Pediatric Cystic Fibrosis patients (ages 10-25 years) will wear a continuous glucose monitor (Dexcom G7) for up to 10 days within 3 months of an annual Oral Glucose Tolerance Test (OGTT) and complete a survey to evaluate correlations between CGM parameters and OGTT values and assess patient/guardian preferences for CFRD screening methods.

Continuous glucose monitors, such as Dexcom, have been established as a standard component of clinical care for continuous blood glucose monitoring. These devices are widely utilized in diabetes management clinics and demonstrate a robust safety and efficacy profile. The intervention also includes administration of a patient preference survey as outlined in the study protocol.

연구는 무엇을 측정합니까?

주요 결과 측정

결과 측정
측정값 설명
기간
Average Blood Glucose Level from Continuous Glucose Monitoring
기간: Up 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)

Up to 10 days of CGM wear (within 3 months of the Oral Glucose Tolerance Test).

2차 결과 측정

결과 측정
측정값 설명
기간
Percentage of Time Glucose Exceeds 150 mg/dL from Continuous Glucose Monitoring
기간: Up 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 (%)

Up to 10 days of CGM wear (within 3 months of the Oral Glucose Tolerance Test).
Percentage of Time Glucose Exceeds 180 mg/dL from Continuous Glucose Monitoring
기간: Up 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 (%)

Up to 10 days of CGM wear (within 3 months of the Oral Glucose Tolerance Test).
Fasting Plasma Glucose Level from Oral Glucose Tolerance Test
기간: Single 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)

Single measurement at the start of the OGTT (within 3 months of CGM wear).
1 hour Plasma Glucose Level from Oral Glucose Tolerance Test
기간: Single 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)

Single measurement 1 hour after glucose load (within 3 months of CGM wear).
2-Hour Plasma Glucose Level from Oral Glucose Tolerance Test
기간: Single 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)

Single measurement 2 hours after glucose load (within 3 months of CGM wear).
Forced Expiratory Volume in 1 Second (FEV1) as a Percentage of Predicted
기간: Within 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. (%)

Within 3 months of CGM placement (standard of care assessment).
Forced Vital Capacity (FVC) as a Percentage of Predicted
기간: Within 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 (%)

Within 3 months of CGM placement (standard of care assessment).
Hemoglobin A1c (HbA1c) Level
기간: At the time of OGTT (within 3 months of CGM wear).

A measure of average blood glucose level (%)

At the time of OGTT (within 3 months of CGM wear).
Body Mass Index (BMI) Z-Score
기간: Within 3 months of CGM placement (standard of care assessment).

Age- and sex-adjusted Body Mass Index standardized score, reflecting nutritional status (z-score)

Within 3 months of CGM placement (standard of care assessment).
Response to Survey Question on CFRD Screening Preferences
기간: After 10 days of CGM wear

Participant's (and/or parent/guardian's) response to the Likert scale questions regarding preferences for Cystic Fibrosis Related Diabetes

After 10 days of CGM wear

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여기에서 이 연구와 관련된 사람과 조직을 찾을 수 있습니다.

스폰서

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일반 간행물

연구 기록 날짜

이 날짜는 ClinicalTrials.gov에 대한 연구 기록 및 요약 결과 제출의 진행 상황을 추적합니다. 연구 기록 및 보고된 결과는 공개 웹사이트에 게시되기 전에 특정 품질 관리 기준을 충족하는지 확인하기 위해 국립 의학 도서관(NLM)에서 검토합니다.

연구 주요 날짜

연구 시작 (실제)

2025년 6월 23일

기본 완료 (추정된)

2027년 8월 1일

연구 완료 (추정된)

2027년 8월 1일

연구 등록 날짜

최초 제출

2026년 6월 29일

QC 기준을 충족하는 최초 제출

2026년 11월 9일

처음 게시됨 (실제)

2026년 11월 12일

연구 기록 업데이트

마지막 업데이트 게시됨 (실제)

2026년 11월 12일

QC 기준을 충족하는 마지막 업데이트 제출

2026년 11월 9일

마지막으로 확인됨

2026년 10월 1일

추가 정보

이 연구와 관련된 용어

기타 연구 ID 번호

  • 24-0945-CCMC

약물 및 장치 정보, 연구 문서

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예

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예

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