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Sponsors and Collaborators: |
Stanford University Santa Clara Valley Health & Hospital System |
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Information provided by: | Stanford University |
ClinicalTrials.gov Identifier: | NCT00186004 |
We wish to find out if in non-diabetic pregnancies, as well as diabetic pregnancies, additional data obtained by Continuous Glucose Monitoring improves perinatal risk prediction.
Condition | Intervention |
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Insulin Resistance |
Device: Continuous Glucose Monitor |
Study Type: | Observational |
Study Design: | Prospective |
Official Title: | Correlation Between Continuous Glucose Monitoring and Intermittent Glucose Monitoring Values and Pregnancy Outcomes |
Ages Eligible for Study: | 18 Years and older |
Genders Eligible for Study: | Female |
Accepts Healthy Volunteers: | Yes |
Inclusion Criteria::- Pregnant patients under 28 weeks gestation
 Exclusion Criteria:- Pre-gestational diabetes
United States, California | |
Stanford University School of Medicine | |
Stanford, California, United States, 94305 |
Principal Investigator: | Yasser Yehia El-Sayed | Stanford University |
Study ID Numbers: | 78694 |
Study First Received: | September 13, 2005 |
Last Updated: | November 19, 2008 |
ClinicalTrials.gov Identifier: | NCT00186004 |
Health Authority: | United States: Institutional Review Board |
Hyperinsulinism Metabolic Diseases Insulin Resistance Metabolic disorder Glucose Metabolism Disorders |