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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04099134
Other study ID # PaCaReg
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date October 10, 2018
Est. completion date October 2029

Study information

Verified date September 2019
Source University of Ulm
Contact Thomas Seufferlein, MD
Phone +49 731 50044501
Email thomas.seufferlein@uniklinik-ulm.de
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

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


Recruitment information / eligibility

Status Recruiting
Enrollment 5000
Est. completion date October 2029
Est. primary completion date October 2028
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility 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

Study Design


Locations

Country Name City State
Germany Universitätsklinikum Ulm Ulm

Sponsors (1)

Lead Sponsor Collaborator
University of Ulm

Country where clinical trial is conducted

Germany, 

Outcome

Type Measure Description Time frame Safety issue
Primary General assessment of applied therapy modalities in pancreatic cancer First diagnose to death or end of surveillance (5 years after curative resection)
Primary Quality of life in pancreatic cancer patients EORTC QLQ c30 and PAN 26 First diagnose to death or end of surveillance (5 years after curative resection)
Secondary General epidemiologic assessment Epidemiologic questionaire First diagnose to death or end of surveillance (5 years after curative resection)
Secondary Assessment of tumor surveillance in pancreatic cancer patients First diagnose to death or end of surveillance (5 years after curative resection)
Secondary Evaluation of predictive and prognostic markers First diagnose to death or end of surveillance (5 years after curative resection)
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