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Septic ShockNCT04239937

Insulin Resistance in Stress-metabolic Medical Patients

An observational study of Septic Shock and Sepsis, run by Slagelse Hospital at 1 site in Denmark.

Unknown status

Status not confirmed. The sponsor has not verified this record for over two years, so it may be out of date.

Official record
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Trial summary

An observational study on the insulin resistance in sepsis and septic shock patients. Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Septic Shock, Sepsis, Insulin Resistance
How many people
50 participants
Where
1 siteDenmark
Study dates
18 Feb 2020to 27 Aug 2020
Phase
Observational
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 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Study population: Sepsis or septic shock patients.

Who may be able to join

  • Patients with sepsis or septic shock who are admitted to the emergency ward and subsequently transferred to an intensive, intermediate or medical ward at Slagelse Hospital. Patients are diagnosed with sepsis or septic shock based on screening using Sequential (sepsis-related) Organ Failure Assessment (SOFA) or Quick SOFA (qSOFA).
  • Patients must be of legal age.

Who cannot join

  • Patients with diabetes (T1DM or T2DM)
  • Patients with terminal cancer
  • Patients who are already participating in a trial
  • Patients who do not understand and speak danish
  • Patients who are demented
  • Postoperative patients <1 month after surgery
  • Patients who are going through dialysis

Trial locations and contacts

1 site in 1 country.

Peter Gæde contact

phgo@regionsjaelland.dk

Denmark1 site, 1 recruiting
  • Slagelse Hospital

    Slagelse, 4200

    Sarah Duncan, 004561705065, duncans@duncans.dk

    Peter Gæde, phgo@regionsjaelland.dk

    Recruiting

Other trials in Denmark

About this study

An observational study on the insulin resistance in sepsis and septic shock patients.

Read the detailed description

This observational study is inspired by the short-term insulin resistance and hyperglycemia that have been demonstrated in post-operative patients in response to tissue injury by Van den Berghe et al 2001. This short-term insulin resistance and hyperglycemia have also been observed in acutely ill patients (Van den Berghe et al 2006). The underlying mechanism for why acute ill patients have short-term insulin resistance is still unclear, but it is believed that the basic mechanism is increased glucose regeneration and gluconeogenesis, which is the consequence of stress metabolism. Hyperglycemia can occur as a result of insulin resistance and is associated with an increased risk of multiple complications, which is why it is important to detect and treat (Van den Berghe et al 2001). This also means that the more insulin-resistant the patient has been prior to the acute condition, the greater the risk of elevated blood glucose concentrations. PRS Review Comments identify apparent errors, deficiencies, or inconsistencies in the submitted information. Any comments provided should not be considered comprehensive. Advisory comments noted in a previous version of a study record may apply to subsequent versions, even if not repeated. It is the responsibility of the data provider to ensure that the record is consistent with the ClinicalTrials.gov Review Criteria.

The aim of the study is to clarify the degree of insulin resistance in medical patients who are not diagnosed with diabetes. Further it will be clarified how long these patients remain insulin resistant after discharge.

The acute medical patients diagnosed with sepsis or septic shock will be observed during hospitalization and after discharge. Sepsis is defined as life-threatening organ dysfunction caused by dysregulated host response to infection. Because the entire body is affected by an infection, it is expected that this group of patients have a high level of stress metabolism, insulin resistance and increased gluconeogenesis. The hypothesis is that acute medical patients diagnosed with sepsis or septic shock have a level of insulin resistance (days to weeks) and thus an increased risk of hyperglycemia. Insulin resistance is expected to decrease as the patient's condition improves.

The hypothesis is:

Patients with elevated infection levels (CRP and leukocyte count) who are simultaneously diagnosed with sepsis, has peripheral insulin resistance due to stress metabolism.

The pancreas will try to compensate for the peripheral insulin resistance by increasing its secretion of insulin to the bloodstream. C-peptide is excreted in equimolar amounts to insulin, thereby C-peptide becomes an expression of peripheral insulin resistance.

It is assumed that the insulin resistance gradually decreases after discharge and further as the patient's condition improves (CRP and leukocyte counts).

The study design is a prospective follow-up study. The difference in C-peptide will be observed over a time period of 28 days as an expression of the participant's insulin secretion. Futher, the participants' blood glucose will also be observed continuously to find the correlation between the degree of insulin resistance and glucose concentration. In addition, measure the correlation between the degree of infection and the increase in C-peptide concentration.

The primary endpoint is the change in C-peptide (the difference between the maximum concentration and the concentration after 28 days).

Secondary endpoints:

  • The area under the curve for blood glucose level measured over 28 days.
  • Correlation of infection level (CRP/leukocyte count) and increase in C-peptide concentration (dose-response).
  • Correlation between infection rate and insulin resistance.

Patients admitted to the hospital with sepsis or septic shock can be recruited. Patients will be followed for 28 days from admission. The patients will be applied to a continuous flash glucose monitor (FGM) on the first day. Follow-up will be performed by blood sampling of C-peptide, leukocyte count, and CRP. HbA1c will also be measured for the exclusion of diabetes. Blood sampling will be taken both during hospitalization and after discharge. C-peptide will be measured every second day during hospitalization and leukocyte count and CRP will be measured every day during hospitalization. Reading of FGM will be performed on the 14. and on the 28. day where blood sampling of C-peptide, leukocyte count, and CRP also will be measured.

Medical subject headings
Shock, Septic, Sepsis, Insulin Resistance

What is being measured

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

  1. C-peptide

    Changes in C-peptide over time

    Measured: 28 days

Secondary outcomes (3)
  1. Blood glucose level

    The area under the curve for blood glucose level measured over 28 days

    Measured: 28 days

  2. Infection level and C-peptide concentration

    Correlation of infection level (CRP/leukocyte count) and increase in C-peptide concentration (dose-response).

    Measured: 28 days

  3. Correlation between infection rate and insulin resistance.

    Correlation between infection rate and insulin resistance.

    Measured: 28 days

Timeline

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

  1. First posted27 Jan 2020
  2. Study start18 Feb 2020
  3. Primary completion27 Aug 2020 (estimated)
  4. Study completion27 Aug 2020 (estimated)

Resources

More details

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

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Prospective
Enrolment
50 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT04239937
Sponsor's protocol ID
SJ-800
Status last verified
Aug 2020
First submitted
21 Jan 2020
Last updated
14 Aug 2020
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No

Questions about this trial

What is this clinical trial studying?

An observational study of Septic Shock and Sepsis, run by Slagelse Hospital at 1 site in Denmark.

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 2 inclusion and 7 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: status not confirmed, as of the sponsor's last update on 14 Aug 2020. 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 Denmark. 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?

Results are not available in the source record.

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

Contact Sarah Duncan (0045 61705065, duncans@duncans.dk), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

C-peptide (time frame: 28 days). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
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 14 Aug 2020.

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