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PACAREG: a Multicenter Registry Trial in Pancreatic Ductal Adencarcinoma

PaCaReg: A Multicenter Registry Trial for the Assessement of Clinical, Epidemiological and Biological Profiles in Patients With Pancreatic Ductal Adenocarcinoma

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04099134
Acronym
PaCaReg
Enrollment
5000
Registered
2019-09-23
Start date
2018-10-10
Completion date
2029-10-31
Last updated
2019-09-25

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

Conditions

Pancreas Adenocarcinoma, Pancreas Cancer

Brief summary

PaCaReg is a multicenter registry trial aiming in the assessement of clinical, epidemiological and biological profiles in patients with pancreatic ductal adenocarcinoma

Interventions

None listed

Sponsors

University of Ulm
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
PROSPECTIVE

Eligibility

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

Inclusion criteria

* Treatment naive histologically or cytologically proven pancreatic ductal adenocarcinoma (PDAC) or highly suspicious diagnosis (only pre-curative-intended resection) * Age =\>18 years * written informed consent

Exclusion criteria

* papillary cancer * neuroendocrine pancreatic tumors

Design outcomes

Primary

MeasureTime frameDescription
General assessment of applied therapy modalities in pancreatic cancerFirst diagnose to death or end of surveillance (5 years after curative resection)
Quality of life in pancreatic cancer patientsFirst diagnose to death or end of surveillance (5 years after curative resection)EORTC QLQ c30 and PAN 26

Secondary

MeasureTime frameDescription
General epidemiologic assessmentFirst diagnose to death or end of surveillance (5 years after curative resection)Epidemiologic questionaire
Assessment of tumor surveillance in pancreatic cancer patientsFirst diagnose to death or end of surveillance (5 years after curative resection)
Evaluation of predictive and prognostic markersFirst diagnose to death or end of surveillance (5 years after curative resection)

Countries

Germany

Contacts

Primary ContactThomas Seufferlein, MD
thomas.seufferlein@uniklinik-ulm.de+49 731 50044501

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026