RECRUITING

CGM-Assisted Management of PN

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

The purpose of this study is to learn more about changes in glucose levels in hospitalized infants with intestinal failure receiving parenteral nutrition or PN (nutrients delivered intravenously), as they transition from continuous PN (given 24 hours a day) to cycled PN (given less than 24 hours a day). There is an increased risk of glucose abnormalities with cycled PN, which can be harmful to infant growth and brain health. Continuous glucose monitors (CGM) will be used to measure interstitial glucose levels (in the tissue under the skin), which are similar to blood glucose levels. CGM is a small, minimally-invasive sensor worn on the thigh, which gives a glucose measurement every 5 minutes, and can help us understand changes in blood sugar levels without having to do a blood draw or fingerstick. CGM will be used during PN cycling for up to 30 days or until hospital discharge. If target GIR cycled PN is not reached following 3 sensor periods (up to 10 days per sensor), the parent/guardian will be approached to accept or decline participation in an optional extension phase. In the extension phase, the primary study will be repeated and CGM monitoring will continue until target GIR cycled PN is reached, up to an additional 3 sensor placements. CGM data will be hidden from the clinical team, there will be no change to routine clinical care. CGM may provide false low glucose readings when the tissue around the sensor is compressed (compression lows), such as when laying on the sensor during sleep. We will generate data during the study to help identify and filter the final dataset to remove likely compression lows. This study may help us understand how cycled PN affects glucose levels in infants with intestinal failure, which may help other children treated with cycled PN in the future.

Official Title

CAMP: CGM-Assisted Management of PN

Quick Facts

Study Start:2023-07-06
Study Completion:2025-08
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT05902104

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:2 Months to 18 Months
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:CHILD
Inclusion CriteriaExclusion Criteria
  1. * Diagnosis of intestinal failure with PN dependence
  2. * Hospitalized at Boston Children's Hospital
  3. * Age: 60 days to 18 months
  4. * Corrected gestational age: greater than or equal to 40 weeks
  5. * Weight: greater than or equal to 4kg
  6. * Likely to proceed to PN cycling within the next month, as assessed by the clinical team
  1. * Underlying medical conditions or medications that predispose to hypoglycemia or hyperglycemia (e.g. insulin administration, systemic glucocorticoids, hyperinsulinism, adrenal insufficiency, other metabolic diseases)
  2. * Diffuse skin disease such that placement of a CGM sensor would be unsafe or difficult to secure
  3. * Known history of allergy or severe reaction to the adhesive/tape that is used to secure the CGM
  4. * Diffuse body edema that would limit accuracy of CGM sensor
  5. * Poor peripheral perfusion or use of vasoactive agents that would limit accuracy of CGM sensor
  6. * Use of medications that interfere with CGM accuracy (e.g. Hydroxyurea, acetaminophen at more than a maximum dose of 1 g every 6 hours up to 4 g every 24 hours)
  7. * Enrolled in competing clinical trial
  8. * Ward of the state

Contacts and Locations

Study Contact

Jessica L Ruiz, MD
CONTACT
617-355-7241
jessica.ruiz@childrens.harvard.edu

Principal Investigator

Michael SD Agus, MD
PRINCIPAL_INVESTIGATOR
Boston Children's Hospital

Study Locations (Sites)

Boston Children's Hospital
Boston, Massachusetts, 02115
United States

Collaborators and Investigators

Sponsor: Boston Children's Hospital

  • Michael SD Agus, MD, PRINCIPAL_INVESTIGATOR, Boston Children's Hospital

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2023-07-06
Study Completion Date2025-08

Study Record Updates

Study Start Date2023-07-06
Study Completion Date2025-08

Terms related to this study

Keywords Provided by Researchers

  • Intestinal Failure
  • Parenteral Nutrition
  • Continuous Glucose Monitoring
  • Hypoglycemia
  • Hyperglycemia

Additional Relevant MeSH Terms

  • Intestinal Failure
  • Hypoglycemia
  • Hyperglycemia