Status:

COMPLETED

Optimization of Glycemic Control in the Hospital and Critical Care Setting

Lead Sponsor:

Ohio State University

Conditions:

Hyperglycemia

Diabetes Mellitus

Eligibility:

All Genders

18+ years

Brief Summary

Continuous Glucose Monitoring collected using the iPro device, to complete a large dataset consisting of routine electronic health records, biological, neurophysiological, physiological, and glycemic ...

Detailed Description

Although recent advances in technology such as electronic medical records and continuous glucose monitoring provide enhanced monitoring capabilities, optimal glycemic control in the hospital and criti...

Eligibility Criteria

Inclusion

  • Male or Female, ≥ 18 years of age.
  • Subject able to provide written informed consent to participate in the study.
  • Female subject with a negative urine or serum pregnancy test, or not of childbearing potential, defined as surgically sterile due to bilateral tubal ligation, bilateral oophorectomy or hysterectomy; or are postmenopausal for at least 1 year.
  • Have a blood sugar value of \>140 mg/dL or an glycosylated hemoglobin A1C (HbA1C) values \>6.5% upon admission to the surgical Intensive Care Unit (ICU), medical ICU, or cardiovascular ICU, and have or not have been diagnosed with type 1 or type 2 diabetes.

Exclusion

  • Subjects younger than 18 years old.
  • Subjects who are prisoners.
  • Subjects with known hypersensitivity to latex or tape.
  • Females who are pregnant or breastfeeding.
  • Subjects unable to provided informed consent.
  • Subjects unable to participate in the study for any reason in the opinion of the Principal Investigator.
  • Subjects enrolled in other research studies.

Key Trial Info

Start Date :

August 19 2014

Trial Type :

OBSERVATIONAL

Allocation :

ACTUAL

End Date :

February 4 2021

Estimated Enrollment :

127 Patients enrolled

Trial Details

Trial ID

NCT04015388

Start Date

August 19 2014

End Date

February 4 2021

Last Update

February 11 2021

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