SiCa-Flam: Perioperative Sitagliptin Medication for Reduction of the Inflammatory Response Associated With Cardiopulmonary Bypass

Sponsor
University Hospital Muenster (Other)
Overall Status
Recruiting
CT.gov ID
NCT05725798
Collaborator
(none)
30
1
45.4
0.7

Study Details

Study Description

Brief Summary

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.

Condition or Disease Intervention/Treatment Phase

Detailed Description

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.

Study Design

Study Type:
Observational
Anticipated Enrollment :
30 participants
Observational Model:
Case-Control
Time Perspective:
Prospective
Official 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
Actual Study Start Date :
Jun 1, 2019
Anticipated Primary Completion Date :
Mar 1, 2023
Anticipated Study Completion Date :
Mar 15, 2023

Arms and Interventions

Arm Intervention/Treatment
DM and Sitagliptin treatment

Cardiac surgery patients who suffer from diabetes mellitus type 2 and take Sitagliptin.

Drug: Sitagliptin
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.

DM without Sitagliptin treatment

Cardiac surgery patients who suffer from diabetes mellitus type 2 and do not take Sitagliptin.

No DM

Cardiac surgery patients who do not suffer from diabetes mellitus type 2 and do not take Sitagliptin.

Outcome Measures

Primary Outcome Measures

  1. Total norepinephrine-requirement within 24 hours after surgery [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 [Retrospective data collection 24 hours after surgery]

    Retrospective data collection from the hospital information system

Secondary Outcome Measures

  1. Immune cells surface markers [Measured 24 hours after surgery]

    Measured by using Cytec Aurora Flow Cytometry

  2. Cytokine-levels [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 [Measured immediately after surgery and 24 hours after surgery]

    Measured by using videomicroscopy to generate sublingual microcirculatory images.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
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

Contacts and Locations

Locations

Site City State Country Postal Code
1 University Hospital Münster Münster North Rhine-Westphalia Germany 48147

Sponsors and Collaborators

  • University Hospital Muenster

Investigators

  • Study Director: Nana-Maria Wagner, Prof. Dr., University Hospital Münster

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Sebastian Kintrup, Principal Investigator, University Hospital Muenster
ClinicalTrials.gov Identifier:
NCT05725798
Other Study ID Numbers:
  • 02-AnIt-19
First Posted:
Feb 13, 2023
Last Update Posted:
Feb 13, 2023
Last Verified:
Feb 1, 2023
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Sebastian Kintrup, Principal Investigator, University Hospital Muenster
Additional relevant MeSH terms:

Study Results

No Results Posted as of Feb 13, 2023