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Perioperative Immune Function and Clinical Complications in Pancreaduodenectomy

Perioperative Immune Function and Clinical Complications in Pancreaduodenectomy

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04774198
Enrollment
58
Registered
2021-03-01
Start date
2021-02-01
Completion date
2024-01-07
Last updated
2026-06-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Pancreas Cancer

Brief summary

Perioperative immunologic signatures can predict the risk of postoperative complications. The results will be puplished as two smanuscripts. The manuscript will focus on preoperative immunologisk data,the second manuscript will include both pre- and postoperative data.

Detailed description

OBJECTIVE Establish evidence for perioperative immunologic risk stratification of patient's risk for clinically postoperative inflammatory complications as a basis for future mechanism-based intervention studies. Combining detailed immune assessment from cell-receptors to cell expression, cytokines, and complications with a temporal aspect is innovative and provides highly warranted novel multidimensional immunological insight. METHODS Adult patients scheduled for PD on the suspicion of pancreatic cancer excluding patients receiving immunomodulating treatment 1 month properatively and/or autoimmune diseases. Patients scheduled for simultaneous procedures on major blood vessels, and/or adjacent organs (spleen, liver) are also not included. Inoperable patients, for instance, due to carcinosis, circulatory/ventilatory instability hindering procedure completion and/or concomitant surgery on major blood vessels, spleen, or liver, are excluded post-inclusion and will not be part of the primary analysis. Patients eligible for inclusion will be identified before their appointment at the Gastrosurgical Dept., Rigshospitalet which is the largest DK and North-European center with about 200 PD/yr annually. Primary outcome: Persistent postoperative hypotension, defined as need for vassopressor infussion on the morning after surgery to maintain middle arterial bloodpressure \>65 mmHg

Interventions

DIAGNOSTIC_TESTblood sample

Blood samples are collected within 24 hours before the surgical procedure, on postoperative day two and seven. Samples collected are as following: TruCulture, flow cytometry, markers of systemic inflammation (Plasma level of pro- and anti-inflammatory molecules assed by Olink inflammation panel, leucocytes, differential count, hemoglobin, thrombocytes and CRP)

Sponsors

Rigshospitalet, Denmark
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Scheduled for PD on the suspicion of pancreatic cancer * Patients able to follow standardised surgical procedure including TIVA anaesthesia with epidural

Exclusion criteria

* Bilirubin \>100 µmol/ltr * Patients receiving immunomodulating treatment 1 month properatively and/or autoimmune diseases and patients non-cenacerous cystic lessions * Patients scheduled for simultaneous procedures on major arterial blood vessels, and/or adjacent organs (spleen, liver) * Inoperable patients, for instance, due to carcinosis, circulatory/ventilatory instability hindering procedure completion and/or concomitant surgery on major arterial blood vessels, spleen, or liver, are excluded post-inclusion and will not be part of the primary analysis * ongoing treatment with glucocortocoid, anti-tnf-alpha etc. * patients diagnosed with rheumatological diseases, IBD or chronic infection (eg. HIV)

Design outcomes

Primary

MeasureTime frameDescription
Number of patients with persistent postoperative hypotension (<65 mmHg) after surgery24 hoursNeed for vasopressor infusion (noradrenaline) to maintain middle arterial blood pressure \>65 mmHg, the morning after pancreaticoduodenectomy.

Secondary

MeasureTime frameDescription
Number of patients with infection30 daysEx. surgical site infection, pneumonia, sepsis, etc, based upon international criteria (eg. center for disease control)
Number of patients with occurrence (yes/no) of systemic inflammatory response syndrome (SIRS) at any time during the first 30 days30 daysSIRS defined as two or more of either of the following four criteria: i) temperature \<36°C or \>38°C, ii) heart rate \>90/min., iii) respiratory rate \>20/min and/or iv) white blood cell count (WBC) \<4x109/L (\<4000/mm³), \>12x109/L (\>12,000/mm³) or ≥10% bands neutrophils.
Number of patients with severe clinical intra- and postoperatove complications30 daysComplications assessed by Clavien-Dindo classification and Comprehensive Clinical complication Index (CCI) ( (i.e. anastomotic leakage, reoperation, thrombosis, bleeding, etc.)
Number of patients with severe clinical intra- and postoperative complications30 daysComplications assessed by SOFA score including single organ system deviation
Number of patients with severe perioperative physiological deviations30 daysFrequency og physiological deviation Monitored by WARD-clinical support system (i.e hypotension, desaturation, tachycardia, etc.).
Number of patients with development of delirium after surgery7 daysDevelopment of delirium measured with the 3D-CAM score

Countries

Denmark

Contacts

STUDY_CHAIREske K Aasvang, DMSci

Rigshospitalet, Denmark

STUDY_DIRECTORSisse R Ostrowski, DMSci

Rigshospitalet, Denmark

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jun 13, 2026