Actively Recruiting
Institut Paoli Calmettes Hepatic Surgery Database
Led by Institut Paoli-Calmettes · Updated on 2018-09-26
3000
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are collecting data from patients undergoing liver surgery for benign liver tumors, primary liver cancer, or secondary liver cancer at Institut Paoli-Calmettes. This observational study aims to create a database to describe the epidemiology of these patients over a period of 5 years. The research helps improve understanding of liver surgery outcomes in different patient groups. The study involves collecting detailed information before, during, and after liver surgery. This includes pre-operative, surgical, and post-surgical data from patients treated at Institut Paoli-Calmettes. There are no experimental treatments, as the study focuses on gathering and analyzing medical data related to liver surgeries. Participants will have their medical and surgical information recorded and monitored as part of routine care. Researchers will analyze this data to describe patterns and outcomes associated with liver surgeries. The study is planned to continue until November 2030, allowing for long-term data collection and follow-up. Participation does not involve additional procedures beyond standard surgical care.
CONDITIONS
Brief Title
Institut Paoli Calmettes Hepatic Surgery Database
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patient undergoing liver surgery for benign liver tumor, primary or secondary liver cancer
You will not qualify if you...
- Patient refusal
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 - Duration of hospital stay after surgery
Participants undergo liver surgery and immediate care following the procedure.
1 surgical visit and hospital stay
Duration - Up to 5 years
Participants are followed after surgery to monitor recovery and collect post-surgical data.
Periodic follow-up visits over 5 years
Trial Site Locations
Total: 1 location
1
Institut Paoli Calmettes
Marseille, Bouches Du Rhone, France, 13009
Actively Recruiting
Research Team
D
Dominique Genre, MD
S
Sandra Cournier
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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