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DiabetesNCT03314272

Automated vs Conventional Perioperative Glycemic Control in Diabetic Patients Undergoing Cardiopulmonary Bypass Surgery

A study of Diabetes and Cardiopulmonary Bypass, run by American University of Beirut Medical Center at 1 site in Lebanon.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

The purpose of this randomized controlled trial is to evaluate a fully automated algorithm for the establishment of glycemic control in diabetic patients and to compare the results with routine management of hyperglycemia in patients undergoing cardiopulmonary bypass surgery. Read more about this study

Who is it for?
Ages 40 to 75 years
Conditions the study is for
Diabetes, Cardiopulmonary Bypass
Could I receive a placebo?
No, everyone receives an active treatment
How many people
59 participants
Where
1 siteLebanon
Study dates
16 May 2018to 4 Feb 2021
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 40 to 75 years
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Type I or type II diabetic patients from both genders aged between 40 - 75 years, who are ASA III-IV undergoing Cardiopulmonary Bypass surgery under general anesthesia for more than 4 hours and requiring the insertion of an arterial line.

Who cannot join

  • Critically ill patients ASA V
  • Pregnant patients
  • Patients' refusal to consent
  • Emergency or lifesaving cases

Trial locations and contacts

1 site in 1 country.

Lebanon1 site
  • American University of Beirut Medical Center

    Beirut

Other trials in Lebanon

About this study

Official title: Automated Versus Conventional Perioperative Glycemic Control in Adult Diabetic Patients Undergoing Cardiopulmonary Bypass Surgery

The purpose of this randomized controlled trial is to evaluate a fully automated algorithm for the establishment of glycemic control in diabetic patients and to compare the results with routine management of hyperglycemia in patients undergoing cardiopulmonary bypass surgery.

Read the detailed description

Upon admission of the patients to the hospital, demographic and physiological data will be collected including waist circumference and BMI. A set of baseline laboratory tests will be done for each patient including: glucose level, Hba1c, lipid profile, creatinine level, liver enzymes and micro albumin/creatinine urinary ratio.

Patients will be asked about the presence of any diabetes complications: nephropathy, retinopathy and/or neuropathy.

In the induction room, an intravenous cannula will be inserted by an experienced anesthesiology staff or resident. A three way stopcock will be connected directly to the cannula. Standard monitors (ECG, non-invasive blood pressure and oxygen saturation) will be connected to the patient. An arterial line will be inserted by the anesthesia resident under sterile conditions using 20 gauge angiocatheter.

General anesthesia will be started. A baseline glucose level will be taken from a blood gas sample, from the arterial line inserted at the beginning of the surgery.

In the Control group, patients' glucose levels will be managed as per the anesthesiologist and/or the anesthesia resident in charge of intraoperative anesthesia management of the patients. The patient will be given actrapid insulin using the glucose sliding scale for diabetic patients as set by the protocol set at AUBMC (mentioned in methodology).

The anesthesia resident will be just asked to take a blood gas sample for the patient every 30 minutes without telling him/her about the purpose of the study, so he/she will be blinded and will act accordingly (including administering insulin to the patient or just monitoring the blood glucose levels without intervening). At the end of the surgery a copy of the blood gas samples and chart of the patients will be collected.

In the Experimental group, patients will be treated using an automated protocol consisting of an insulin infusion pump named The Space Glucose Control System by B. Braun, in Melsungen, Germany. The Space Glucose Control system is a Class IIb medical device. The manufacturer, B. Braun, received the first CE mark in June 2004. The most recent renewal was in May 2013. At the bottom of this system, a central user interface is connected with a touch screen interface in order to enter the data. The glucose reading as measured has to be entered manually by the medical house staff (anesthesia resident) via the touch screen display. Based on this input the system gives advice on the insulin infusion rate. The suggested insulin infusion is displayed on the screen, but has to be entered manually and therefore confirmed by the medical staff.

For glucose measurement, a sample of blood gas will be taken every half an hour. Actrapid HM will be used in a 4IU/ ml concentration for infusion in a 50 ml syringe.

The range of glucose will be recorded throughout the intra-operative period. The number of hypoglycemic (<70mg/dl) and hyperglycemic (> 200mg/dl) events will be recorded.

Insulin allergy in patients with diabetes mellitus is a rare condition. Signs and symptoms including angioedema, hypotension, urticaria and rash, if present, are usually noticed immediately following the injection. Patients suspected of having insulin allergy will be treated by stopping the infusion, administering antihistaminic H2 and H1 blockers, corticosteroids and pressors depending on the magnitude of the allergic reaction.

Hypoglycemia defined as blood glucose level less than 70 mg/dl, will be detected and treated promptly to provide a rise in blood glucose to a safe level in order to eliminate any potential harm. The intervention will include intravenous infusion of 100 to 200 ml of D5 water over 1 to 3 minutes and repeating blood glucose level after 15 minutes to reach a target blood sugar of 100. The same intervention will be repeated in case this level wasn't reached and patient will be withdrawn from the study after two failed correction and will be treated more aggressively with an infusion of D10W.

Being tested
Space Glucose Control
Medical subject headings
Diabetes Mellitus

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Space Glucose ControlDevice

    Development of a closed loop control system via Space Glucose Control that automatically infuses insulin on the basis of an automated algorithm, which integrates a continuous glucose signal, could help overcome these obstacles and permit strict glycemic control without increasing the workload.

Study groups in NCT03314272
Study groupRoleWhat they receive
Sliding scale protocolNo interventionConsists of giving insulin every 30 minutes based on the blood glucose readings as follows: * <150 mg/dl: 0 units of insulin * 150-220 mg/dl: 2 units of insulin * 201-250 mg/dl: 4 units * 251-300 mg/dl: 6 units * 301-350 mg/dl: 8 units * 351-400 mg/dl: 10 units * > 400 mg/dl: inform the MD on call
Space Glucose ControlExperimentalAutomated protocol consisting of an insulin infusion pump named The Space Glucose Control System. Intervention: For glucose measurement, a sample of blood gas will be taken every 30 minutes. Actrapid HM will be used in a 4IU/ ml concentration for infusion in a 50 ml syringe. The range of glucose will be recorded throughout the intra-operative period. The number of hypoglycemic (<70mg/dl) and hyperglycemic (> 200mg/dl) events will be recorded.
Receives: Device: Space Glucose Control

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Percentage of patients who will have a serum glucose level between 140-180mg/dl during surgery.

    The reduction of this percentage to less than 10% with the fully automated algorithm as clinically significant

    Measured: Throughout the surgery period and postoperatively (admission to the CSU)

  2. Percentage of patients who had hyperglycemic events

    At least one hyperglycemic event over the surgery time

    Measured: Throughout the surgery periodThroughout the surgery period and postoperatively (admission to the CSU)

  3. Percentage of patients who had hypoglycemic events

    At least one hypoglycemic event over the surgery time

    Measured: Throughout the surgery periodThroughout the surgery period and postoperatively (admission to the CSU)

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted19 Oct 2017
  2. Study start16 May 2018
  3. Primary completion4 Feb 2021
  4. Study completion4 Feb 2021

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
Single blind
Who is masked
Participant
Enrolment
59 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT03314272
Sponsor's protocol ID
ANES.RK.03
Status last verified
Dec 2021
First submitted
16 Oct 2017
Last updated
3 Jan 2022
Results posted
No
FDA-regulated drug
No
FDA-regulated device
No

Publications

  • Bellon F, Sola I, Gimenez-Perez G, Hernandez M, Metzendorf MI, Rubinat E, Mauricio D. Perioperative glycaemic control for people with diabetes undergoing surgery. Cochrane Database Syst Rev. 2023 Aug 1;8(8):CD007315. doi: 10.1002/14651858.CD007315.pub3.

    PubMed 37526194
  • Kaddoum R, Khalili A, Shebbo FM, Ghanem N, Daher LA, Ali AB, Chehade NEH, Maroun P, Aouad MT. Automated versus conventional perioperative glycemic control in adult diabetic patients undergoing open heart surgery. BMC Anesthesiol. 2022 Jun 16;22(1):184. doi: 10.1186/s12871-022-01721-6.

    PubMed 35710339

Questions about this trial

What is this clinical trial studying?

A study of Diabetes and Cardiopulmonary Bypass, run by American University of Beirut Medical Center at 1 site in Lebanon.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 1 inclusion and 4 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 3 Jan 2022. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Lebanon. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Percentage of patients who will have a serum glucose level between 140-180mg/dl during surgery. (time frame: Throughout the surgery period and postoperatively (admission to the CSU)). The study lists 3 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT03314272, which also lists 2 linked publications.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 3 Jan 2022.

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