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NCT Number: NCT04834518

Screening for Islet Autoantibodies in the Israeli Paediatric General Population for Detection of Pre-symptomatic Type-1 Diabetes Mellitus

A national screening program for children aged 9 months-5 years that will be tested for the presence of islet autoantibodies.Up to 50,000 Children will be screened by their primary care physician all over Israel. The initial screening will be done at the age of 1 year (in conjunction with the routinely collection of blood for CBC ) and repeated at ages 2-5 years. Antibodies will be measured in capillary blood samples using the Ultrasensitive Antibody Detection by Agglutination-PCR (ADAP) technology developed by Enable Biosciences, which is 1,000-10,000 times more analytically sensitive than currently used methods. By using this innovative technology in such a large cohort, the study is anticipated to detect antibodies at an unprecedented earlier age.When positive in the screening, multiple antibodies will be confirmed by a second sample analyzed by the ADAP technology. In addition, multiple antibodies will be also measured using a radio-binding assay (RBA) of a venous blood sample for investigational purpose only. Children with confirmed multiple antibodies (stage 1 or 2 T1D) will be followed up routinely for the appearance of clinical signs of diabetes (HbA1c, repeated OGTT, monitoring of urine and blood glucose where indicated) and will be invited along with their families to attend an educational program. This program will include diabetes education emphasizing on DKA prevention as well as stress assessment for the families involved and stress alleviating interventions. The analysis and storage of the samples will be done in a single screening center at Schneider Children's Medical Center of Israel.

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Key information

Conditions

Age range

9 month–5 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Soroka Medical Center, Beersheba, Israel

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Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Informed consent obtained before any trial-related activities
  • Children aged 9-months- 5 years at first screening.

Exclusion criteria

  • Known diagnosis of diabetes (Type 1 or other)

Treatment and study plan

Primary outcomes

  1. Diagnosis of presymptomatic type 1 diabetes

    Time frame: End of screening and follow-up period-4 years after obtaining the first screening test

    Presymptomatic type 1 diabetes, defined as positive for 2 or more islet autoantibodies (GADA, IA-2A, and IAA) or those with high levels of a single antibody in both the screening and confirmation samples or in the screening sample plus a diagnosis of diabetes prior to obtaining the conformation sample.

    Presymptomatic type 1 diabetes will be classified as stage 1, 2, or 3:

    • Stage 1 will be defined as 2 or more islet autoantibodies or high levels of a single antibody and normal glucose tolerance based on OGTT results. (not including patients with only a single antibody who have first degree relative with type 1 diabetes)
    • Stage 2 will be defined as 1 or more islet autoantibodies accompanied by dysglycemia (fasting plasma glucose of 110-125 mg/dL or impaired 2-hour plasma glucose of 140- 199 mg/dL and/or plasma glucose ≥200 mg/dL at intermediate time points [30, 60, 90 minutes]) based on OGTT results.
    • Stage 3 will be defined according to the American Diabetes Association criteria
  2. Frequency of Diabetic Ketoacidosis on the clinical presentation of Type 1 Diabetes

    Time frame: End of screening and follow-up period-4 years after obtaining the first screening test

Secondary outcomes

  1. The average age of islet autoantibody seroconversion

    Time frame: End of screening and follow-up period-4 years after obtaining the first screening test

  2. The rate of islet autoantibody seroconversion

    Time frame: End of screening and follow-up period-4 years after obtaining the first screening test

  3. The rate of progression from pre-symptomatic T1D to clinical diabetes

    Time frame: End of screening and follow-up period-4 years after obtaining the first screening test

Study contacts

Contact information is provided by the study sponsor or research team.

Alona Hamou, MSc

CONTACT

[email protected]

972-545-950-277

Moshe Phillip, Prof

CONTACT

[email protected]

972-544-795-995

Sponsors and collaborators

Lead sponsor

Rabin Medical Center

Other

Collaborators

  • Juvenile Diabetes Research Foundation

Registry information

Acronym: ADIR

Important dates

Study start
2021
Primary completion
2027
Study completion
2027
First posted
Apr 8, 2021
Registry last updated
Oct 17, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

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This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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