Establishing a Pediatric Reference Range for the 13C-Spirulina Gastric Emptying Breath Test (GEBT)

Sponsor
Cairn Diagnostics (Industry)
Overall Status
Recruiting
CT.gov ID
NCT06004596
Collaborator
Medical College of Wisconsin (Other), Baylor College of Medicine (Other)
300
3
2
19.5
100
5.1

Study Details

Study Description

Brief Summary

The goal of this clinical trial is to define the normal response to the 13C-Spirulina Gastric Emptying Breath Test (GEBT) in children, so that we can use this test to help diagnose children that are suspected of having a condition called gastroparesis, which means that food doesn't empty from their stomach normally.

Participants will blow into test tubes to collect breath samples before and after eating a scrambled egg GEBT meal that contains a small amount of specially grown Spirulina (a blue-green alga used as a dietary supplement) that contains mostly carbon-13 (a non-radioactive kind of carbon atom). Analysis of the amount of 13C in the carbon dioxide in breath before and after eating the GEBT meal can measure how fast food is emptying from the stomach.

Condition or Disease Intervention/Treatment Phase
  • Diagnostic Test: 13C-Spirulina Gastric Emptying Breath Test (GEBT)
  • Diagnostic Test: 13C-Spirulina Gastric Emptying Breath Test (GEBT) - repeat
N/A

Detailed Description

Children will complete questionnaires to ensure that they are qualified to enter the study and are likely to have normal gastric emptying rates. Informed consent/assent will be obtained.

Breath samples will be collected by children blowing into test tubes before and after eating a 13C-Spirulina GEBT meal. Breath samples will be collected and the test will be administered via telehealth or at one of the children's hospital clinics.

Researchers will analyze results from different age groups to see if there are differences in normal gastric emptying in younger/older children and boys/girls.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
300 participants
Allocation:
Randomized
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Diagnostic
Official Title:
Establishing a Pediatric Reference Range for the 13C-Spirulina Gastric Emptying Breath Test (GEBT)
Actual Study Start Date :
Mar 17, 2023
Anticipated Primary Completion Date :
Oct 31, 2024
Anticipated Study Completion Date :
Oct 31, 2024

Arms and Interventions

Arm Intervention/Treatment
Other: Reference Range determination

13C-Spirulina Gastric Emptying Breath Test (GEBT) administered to healthy participants

Diagnostic Test: 13C-Spirulina Gastric Emptying Breath Test (GEBT)
Diagnostic test

Active Comparator: Biological Variability

13C-Spirulina GEBT administered a second time to subset of participants to determine pediatric biological variability.

Diagnostic Test: 13C-Spirulina Gastric Emptying Breath Test (GEBT) - repeat
Diagnostic test - repeat for biological variability deterination

Outcome Measures

Primary Outcome Measures

  1. kPCD (kPCD = 1000 x percent dose of 13C excreted) at 15 minutes (min-1) [15 minutes]

    13CO2 excretion rate calculated at 15 minutes after meal completion

  2. kPCD at 30 minutes (min-1) [30 minutes]

    13CO2 excretion rate calculated at 30 minutes after meal completion

  3. kPCD at 45 minutes (min-1) [45 minutes]

    13CO2 excretion rate calculated at 45 minutes after meal completion

  4. kPCD at 60 minutes (min-1) [60 minutes]

    13CO2 excretion rate calculated at 60 minutes after meal completion

  5. kPCD at 90 minutes (min-1) [90 minutes]

    13CO2 excretion rate calculated at 90 minutes after meal completion

  6. kPCD at 120 minutes (min-1) [120 minutes]

    13CO2 excretion rate calculated at 120 minutes after meal completion

  7. kPCD at 150 minutes (min-1) [150 minutes]

    13CO2 excretion rate calculated at 150 minutes after meal completion

  8. kPCD at 180 minutes (min-1) [180 minutes]

    13CO2 excretion rate calculated at 180 minutes after meal completion

  9. kPCD at 210 minutes [210 minutes]

    13CO2 excretion rate calculated at 210 minutes after meal completion

  10. kPCD at 240 minutes (min-1) [240 minutes]

    13CO2 excretion rate calculated at 240 minutes after meal completion

  11. Test meal/test completion [up to 20 minutes]

    Participant was able to successfully consume the meal/complete the test - Measured by determining whether box on test request form checked or not checked and whether or not all breath samples were collected/able to be analyzed

  12. Tmax (mins) [90 to 240 minutes]

    Time of maximum excretion rate - time at which the largest kPCD is observed

Eligibility Criteria

Criteria

Ages Eligible for Study:
7 Years to 18 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Children ages 7 to 18 years who provide written assent and whose parents provide written consent for participation

  • Healthy and without any significant prior medical history or developmental delays

  • Able to eat the test meal and provide breath samples.-

Exclusion Criteria:

Any known physician-diagnosed medical (gastrointestinal, pancreatic, or liver disease that may cause malabsorption, neurological) or psychiatric disease

  • Chronic pulmonary disease including moderate/severe reactive airway disease requiring treatment with a daily inhaler

  • Type 1 or 2 Diabetes

  • Chronic gastrointestinal symptoms or functional gastrointestinal disorders

  • Mental retardation or pervasive developmental disorder

  • Currently receiving prescription drug therapy that may affect gastric motor function or sensation

  • Any over-the-counter or herbal supplements that may affect gastric motor function or sensation

  • Allergy to Spirulina, egg, milk, wheat or gluten (unless consuming gluten free crackers with the test meal) or known intolerance to any ingredient in the test meal

Contacts and Locations

Locations

Site City State Country Postal Code
1 Cairn Diagnostics Brentwood Tennessee United States 37027
2 Texas Children's Hospital/Baylor College of Medicine Houston Texas United States 77030
3 Medical College of Wisconsin Milwaukee Wisconsin United States 53226

Sponsors and Collaborators

  • Cairn Diagnostics
  • Medical College of Wisconsin
  • Baylor College of Medicine

Investigators

  • Principal Investigator: Catherine E Williams, PhD, Cairn Diagnostics

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Cairn Diagnostics
ClinicalTrials.gov Identifier:
NCT06004596
Other Study ID Numbers:
  • CDX-CD-PRO-442
First Posted:
Aug 22, 2023
Last Update Posted:
Aug 22, 2023
Last Verified:
Aug 1, 2023
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
Yes
Product Manufactured in and Exported from the U.S.:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Aug 22, 2023