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NCT06381882Enrolling by invitation

The Role of the Human Microbiome in Patients After Pancreatic Resection.

Establishing the Role of the Human Microbiome in Patients With a Presumed Pancreatic or Periampullary (Pre)Malignancy and Pancreatic Resection.

Source: ClinicalTrials.gov · Last updated 27 Apr 2026

Brief summary (registry, in English)

The goal of this observational study is to classify patients that undergo pancreatic resection for presumed pancreatic or periampullary malignancy into high and low risk groups for postoperative complications based on longitudinal saliva, rectal/faecal, tumor, blood and/or bile microbiome profiles. To identify the dynamics of the microbiome, as well as the possibly related short-term and long-term complications, multiple samples at different timepoints are needed from the patients.

Status (registry)
Enrolling by invitation
Study type
Observational
Enrollment
200 (estimated)
First submitted
25 Feb 2024
Start date
1 Jun 2024
Primary completion date
1 Aug 2026
Lead sponsor
St. Antonius Hospital
NCT number
NCT06381882

What you commit to

  • Study type: Observational
  • Planned participants: 200
  • From 1 Jun 2024 to the primary completion date, 1 Aug 2026
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other

  • Inability to provide adequate informed consent (e.g. language barrier, illiteracy)

Who the study is looking for

  • Adult patient with a resectable, borderline resectable or locally advanced pancreatic and periampullary presumed (pre)malignancy.
  • The intention of the treatment must be curative including surgery and (neo-)adjuvant chemotherapy.
  • Willing and able to adhere to the study procedures described in this protocol and to grant the study team access to the electronic patient file and other data that are required to answer the research questions described in this protocol.

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
St. Antonius Hospital
Coordinator of this site? Confirm its status
NieuwegeinNetherlandsUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.