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NCT03510078

Intensive Versus Conventional Hyperglycemic Control in Hospitalized Non-critically Ill Patients

Recruiting now NA Last updated 11 April 2024
What this trial tests

NA trial testing Insulin in Diabetes Mellitus in 600 participants. Currently enrolling.

Timeline
17 April 2018
Primary endpoint
1 May 2025
1 October 2026

Quick facts

Lead sponsorRabin Medical Center
PhaseNA
StatusRecruiting now
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingdouble
Primary purposetreatment
Enrollment600
Start date17 April 2018
Primary completion1 May 2025
Estimated completion1 October 2026
Sites2 locations across Israel

Drugs / interventions tested

Conditions studied

Sponsor

Rabin Medical Center

Who can join

Adults 18 to 120, any sex, with Diabetes Mellitus or Non-critically Ill Patients. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Hyperglycemia is a common condition among hospitalized patients. The occurrence of severe hyperglycemia is associated with increased morbidity and mortality in several populations. Several trials assessed the benefits of aggressive versus conventional glucose control. These studies evaluated different patient populations, glucose targets and treatment protocols and as a result reported conflicting results. To date there are no clear guidelines regarding to the preferred glucose target range in hospitalized non-critically ill patients. The common practice is to maintain glucose level lower than 180 mg/dl however there are no evidence based regarding to the outcomes of hospitalized patients treated with intensive compared to conventional glycemic control. This prospective randomized controlled study will compare intensive vs. standard glycemic control in hospitalized non-critically ill patients. Within 24 hours of hospitalization in the internal medical or geriatric departments, patients who are expected to require hospitalization for at least three consecutive days will be randomly assigned into one of the two study groups - intensive with a target blood glucose range of 130 mg per deciliter or less, or conventional glucose control, with a target of 130-180 mg per deciliter. The investigators defined the primary end point as a composite outcome of mortality in 30 days, severe hypoglycemia, severe infections within 30 days, CVA and cardiac ischemic events within 30 days.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other trials of Insulin

Trials testing the same drug.

Other recruiting trials for Diabetes Mellitus

Currently open trials in the same condition.

Other Rabin Medical Center trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

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