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Completed

NCT Number: NCT05725798

Perioperative Sitagliptin Medication for Reduction of the Inflammatory Response Associated With Cardiopulmonary Bypass

Sitagliptin is an inhibitor of the enzyme dipeptidylpeptidase-4 (DPP-4) and represents an established drug in type 2 diabetes mellitus treatment. However, Sitagliptin may also have several antiinflammatory properties. Within this study the investigators examine the effects of perioperative Sitagliptin intake on the inflammatory response after cardiopulmonary bypass.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

University Hospital Münster

Münster, North Rhine-Westphalia, 48147, Germany

About this study

Sitagliptin is an inhibitor of the enzyme dipeptidylpeptidase-4 (DPP-4) and represents an established drug in type 2 diabetes mellitus treatment. However, Sitagliptin may also have several antiinflammatory properties. For example, it is known that DPP-4-inhibition prevents procalcitonin from being cleaved to a truncated form that lacks 2 amino acids. As the investigators described recently, truncated procalcitonin targets the CRLR-RAMP1-receptor on vascular endothelium and induces VE-cadherin-phosphorylation which leads to leakage of fluids and proteins from vessels. Furthermore, many other immunoregulatory targets such as substance p, CXCL10 or NF-kB have been reported to be modified by DPP-4. Therefore, it can be assumed that Sitagliptin possibly represents a powerful drug in inflammatory circumstances.

The aim of this study is to prove possible antiinflammatory properties by conducting an observational trial in cardiac surgery patients. All patients undergo cardiac surgery with the use of cardiopulmonary bypass (CBP) which is known to trigger a systemic inflammatory response syndrome (SIRS). Group 1 suffers from diabetes mellitus type two and regularly takes Sitagliptin which is continued perioperatively. Group 2 also suffers from diabetes mellitus type 2 but does not take Sitagliptin. Group 3 has no diabetes mellitus but also undergoes cardiac surgery. To determine the effect of Sitagliptin under inflammatory conditions deep immune phenotyping and a cytokine assay is performed from blood withdrawals 24h after surgery. Moreover, the sublingual microcirculation is measured two times after the operation.

Taking all measurements of the cellular immune system, the humoral immune system and the vasculature into account it should be possible to define the immunoregulatory effects of Sitagliptin treatment more properly.

Who can participate

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age >18 years
  • Patients undergoing cardiac surgery with use of CBP and...
  • Diabetes mellitus type 2 with Sitagliptin treatment or,
  • Diabetes mellitus type 2 without Sitagliptin treatmet or,
  • No diabetes mellitus
  • Written informed consent

Exclusion criteria

  • Diabetes mellitus type 1
  • Treatment with another DPP4-inhibitor
  • Treatment with GLP-1-analoga
  • Emergency surgery
  • Chronic or acute infection
  • Pregnancy
  • Participation in an interventional study trial within last 3 months
  • Relationship to study investigators

Treatment and study plan

Sitagliptin

Drug

Group 1 who regularly takes Sitagliptin due to diabetes mellitus type 2 continues the treatment perioperatively. Group 2 and group 3 do not take Sitagliptin.

Primary outcomes

  1. Total norepinephrine-requirement within 24 hours after surgery

    Time frame: Retrospective data collection 24 hours after surgery

    Retrospective data collection from the hospital information system

  2. Total crystalloid volume-requirement within 24 hours after surgery

    Time frame: Retrospective data collection 24 hours after surgery

    Retrospective data collection from the hospital information system

Secondary outcomes

  1. Immune cells surface markers

    Time frame: Measured 24 hours after surgery

    Measured by using Cytec Aurora Flow Cytometry

  2. Cytokine-levels

    Time frame: Measured 24 hours after surgery

    Measured by using multiplex immunoassay analysis.

  3. Sublingual microcirculatory parameters: Total vessel density, Proportion of Perfused Vessels, Perfused Vessel Density, Microvascular Flow Index

    Time frame: Measured immediately after surgery and 24 hours after surgery

    Measured by using videomicroscopy to generate sublingual microcirculatory images.

Sponsors and collaborators

Lead sponsor

University Hospital Muenster

Other

Registry information

Official study title

Perioperative Sitagliptin Medication for Reduction of the Inflammatory Response Associated With Cardiopulmonary Bypass and Postoperative Glucose Control in Diabetic Patients Undergoing Elective Cardiac Surgery - a Pilot Study

Acronym: SiCa-Flam

Important dates

Study start
2022
Primary completion
2023
Study completion
2023
First posted
Feb 13, 2023
Registry last updated
Aug 22, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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