Actively Recruiting

Age: 18Years +
All Genders
ID04099134

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

Led by University of Ulm · Updated on 2019-09-25

5000

Participants Needed

1

Research Sites

52 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are conducting a multicenter registry trial called PaCaReg to study pancreatic ductal adenocarcinoma, a type of pancreas cancer. The trial aims to understand clinical, epidemiological, and biological profiles in patients with this condition. The study is observational and focuses on collecting data to assess various aspects related to the disease and its treatment. Participants in this study are those diagnosed with pancreatic ductal adenocarcinoma or those with a highly suspicious diagnosis prior to curative surgery. The trial does not involve experimental treatments but gathers information on the therapies patients receive and their outcomes. Data collection spans from the time of diagnosis through up to five years after curative resection, covering therapy modalities, quality of life, tumor surveillance, and predictive markers. During the study, participants' medical information, treatment details, and quality of life will be monitored over time. The researchers will assess outcomes such as survival, therapy effects, and epidemiological factors. This long-term observation helps in understanding the disease better and may guide future care strategies. Participation involves providing informed consent and allowing access to clinical data during the observation period.

CONDITIONS

Brief Title

PACAREG: a Multicenter Registry Trial in Pancreatic Ductal Adencarcinoma

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Treatment naive histologically or cytologically proven pancreatic ductal adenocarcinoma (PDAC) or highly suspicious diagnosis (only pre-curative-intended resection)
  • Age �318 years
  • Written informed consent
Not Eligible

You will not qualify if you...

  • Papillary cancer
  • Neuroendocrine pancreatic tumors

AI-Screening

AI-Powered Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

Long-term Monitoring

Duration - Up to 5 years after curative resection or until death

Participants are observed over time to assess clinical, epidemiological, and biological profiles related to pancreatic ductal adenocarcinoma.

Trial Site Locations

Total: 1 location

1

Universitätsklinikum Ulm

Ulm, Germany

Actively Recruiting

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Research Team

T

Thomas Seufferlein, MD

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

0

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