Actively Recruiting
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
Eligibility Criteria
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
You will not qualify if you...
- Papillary cancer
- Neuroendocrine pancreatic tumors
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
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
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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