RecruitingNot Applicable

Accuracy of Lactate Meter in GSDIa

United States10 participantsStarted 2025-04-14

Plain-language summary

The goal of this observational study is to determine if home lactate meters (both capillary and serum sample) are accurate, compared to lab serum lactate in a population of patients with glycogen storage disease type 1a and to determine if the Accu Chek Guide glucometer (capillary sample) is accurate, in a population of patients with glycogen storage disease type 1a.

Who can participate

Age range0 Years – 60 Years

SexALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * Patients with diagnosed/confirmed (by liver biopsy or genetic testing) Glycogen Storage Disease Type Ia (ICD 10 code: E74.01). * Connecticut Children's Emergency Department visit and/or admission to Connecticut Children's during time study is active * For pediatric participants: Ability of child's parent/legal guardian to understand and the willingness to sign a written informed consent document * For adults: Ability to understand and the willingness to sign a written informed consent Exclusion Criteria: * Patients with Glycogen storage disease unspecified 74.00, or Ib * Patients not meeting inclusion criteria

What they're measuring

Home lactate meter accuracy in GSDIa compared with lab lactate

Timeframe: Every 1-3 hours for a maximum 33 hours

Trial details

NCT IDNCT06843330

SponsorConnecticut Children's Medical Center

Sponsor typeOTHER

Study typeOBSERVATIONAL

Primary completion2027-03-10

Contact for this trial

Malaya Mount, MS, RD

860-837-6700 mmount@connecticutchildrens.org

View on ClinicalTrials.gov More Glycogen Storage Disease Type Ia trials