RecruitingOBSERVATIONAL

Pancreatic Surgical Database

Doctors in France are gathering important medical information from adults who have had surgery for pancreatic cancer. This project, called the Pancreatic Surgical Database, collects details about their surgery and treatment. The main goal is to build a better understanding of pancreatic cancer and the effects of surgery. By looking at this information over time, researchers hope to find new ways to improve treatment and care for patients with this disease. This is a data collection study, meaning it focuses on gathering existing information rather than testing new medicines or treatments.

At a glance

Status

Recruiting

Sponsor

Institut Paoli-Calmettes

Enrolment target

1,500

Start

01 Nov 2014

Pancreatic Neoplasms

What is this study about?

Imagine a big, secure filing cabinet where doctors keep important notes about patients who have had surgery for pancreatic cancer. That's essentially what the Pancreatic Surgical Database is. Doctors from two hospitals in France, Institut Paoli Calmettes and Assistance Publique des Hôpitaux de Marseille, are working together to put information from their patients into this database.

The main idea behind this project is to learn as much as possible from real-life patient experiences. By collecting details about surgeries, how patients recovered, and their overall health, doctors can start to see patterns. For example, they might discover if certain types of surgery work better for some patients, or if particular treatments lead to better outcomes. This kind of information is really valuable because it helps medical professionals make more informed decisions and continuously improve the care they provide to people with pancreatic cancer.

This study isn't about trying new medications or procedures on patients. Instead, it's about carefully reviewing and understanding the treatments that have already been given. It's a way for doctors to pool their knowledge and experience, leading to a clearer picture of how pancreatic cancer is treated and how those treatments affect people in the long run. Ultimately, the goal is to use this gathered wisdom to offer even better care to future patients.

Key takeaways

This study collects information about pancreatic cancer surgery.
It's a database for learning, not testing new treatments.
Only existing medical records are used; no extra visits needed.
Your identify will be kept confidential and secure.
Your participation helps improve care for future patients.
You can choose not to participate or withdraw at any time.

Who may be eligible?

To be part of this study, you must be an adult aged 18 or over. You also need to have had surgery specifically for pancreatic cancer at either Institut Paoli Calmettes or Assistance Publique des Hôpitaux de Marseille in France.

However, there are reasons why you might not be able to join. If you do not want your information to be included or you tell the doctors that you don't wish to take part, then you won't be in the study. Your choice not to participate will always be respected.

Could this study suit you?

Answer these quick questions to see if you may be eligible. This is a guide only — the research team makes the final call.

Are you 18 years old or older?
Have you had surgery for pancreatic cancer?
Was your surgery at Institut Paoli Calmettes or Assistance Publique des Hôpitaux de Marseille in France?
Are you comfortable with your medical information being used anonymously for research?

Answer every question to see your result.

What does participation involve?

If you are eligible and agree to take part in this study, it simply means that information about your medical care and surgery for pancreatic cancer will be added to a secure database. You won't need to attend any extra appointments or receive any new medical tests or treatments because of this study. There are no medications to take, and no special follow-up visits requested specifically for the database. Doctors will use the information already collected during your standard medical care.

Potential risks and benefits

The main benefit of taking part is that the information from your medical journey can help doctors learn more about pancreatic cancer, potentially leading to improved care for others in the future. As this study only involves collecting existing medical information, there are no direct medical risks or side effects from participating. Your identity and personal details will be kept confidential. You always have the right to change your mind and withdraw your permission for your information to be used at any point, without affecting your medical care.

Locations (1)

Institut Paoli Calmettes
Verified postcode
Marseille, France· Recruiting

Common questions

What kind of information will be collected about me?

Doctors will collect medical and surgical details related to your pancreatic cancer and the treatment you received. This is information already in your medical records.

Will my name or personal details be shared?

No, your personal information will be kept confidential. The study focuses on health data, not your identity.

Do I need to do anything extra if I join?

No, there are no extra appointments, tests, or treatments required for this study. It simply involves using your existing medical records.

Can I decide not to be part of the study?

Yes, if you do not want your information included, you can decline to participate. This will not affect your medical care.

How will this study help other patients?

By gathering information from many patients, doctors hope to better understand pancreatic cancer and improve future treatments and care for others.

How to find out more

Dominique Genre, MD

drci.up@ipc.unicancer.fr 0033491223778 Official trial record

Always speak to your GP or specialist before deciding to take part in a study.