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Protocol to Validate the Performance of the Mellitus Glycated CD59 ELISA for Gestational Diabetes Screening

M

Mellitus

Status

Withdrawn

Conditions

Gestational Diabetes

Treatments

Diagnostic Test: Mellitus GCD59 Test

Study type

Observational

Funder types

Other
Industry

Identifiers

NCT03865901
CSP-MEL-002

Details and patient eligibility

About

Demonstrate effective performance of the Mellitus GCD59 Test (an ELISA) in screening for gestational diabetes mellitus (GDM)

Full description

Validate the performance of the Mellitus GCD59 ELISA as a screening test for GDM by evaluating its negative predictive value (NPV) and positive predictive value (PPV) to identify pregnant women at risk for GDM. Sensitivity and specificity of the Mellitus GCD59 ELISA will also be evaluated.

Sex

Female

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Women 18 years of age or older at enrollment
  2. Has an established viable singleton pregnancy
  3. Is recommended for routine GDM screening between 24-28 weeks gestation
  4. Has confirmed gestational age of 24-28 weeks at the Screening Visit
  5. Is willing and able to provide documentation of informed consent

Exclusion criteria

  1. Has diabetes before pregnancy or has already been diagnosed with GDM
  2. Has contraindications for drinking oral glucose solution up to 100 g of sugar
  3. Is taking metformin for any reason
  4. Has any concomitant illness, disease or condition that, in the clinical judgment of the investigator, is likely to prevent the subject from complying with any aspect of the protocol, or that may put the subject at unacceptable risk

Trial design

0 participants in 1 patient group

Non-diabetic pregnant women
Description:
Non-diabetic women with singleton pregnancy undergoing screening for gestational diabetes who provide plasma samples for testing with the Mellitus GCD59 Test
Treatment:
Diagnostic Test: Mellitus GCD59 Test

Trial contacts and locations

19

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Data sourced from clinicaltrials.gov

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