To hear about similar clinical trials, please enter your email below

Trial Title: NON-COlorectal Liver METastases Undergoing Liver Resection

NCT ID: NCT06542926

Condition: Liver Metastases

Conditions: Official terms:
Neoplasm Metastasis
Liver Neoplasms

Study type: Observational [Patient Registry]

Overall status: Not yet recruiting

Study design:

Time perspective: Other

Intervention:

Intervention type: Procedure
Intervention name: liver resection
Description: Resection of non-colorectal liver metastases

Other name: hepatectomy

Summary: Liver metastases (LM) are common in various types of malignant diseases, either at the diagnosis of the primary tumour or at a later time point. While the resection of colorectal LM (CRLM) is a well-established procedure, with survival rates superior to chemotherapy alone, controversial data still exist on liver resection for non-colorectal LM (NCRLM) (2, 3). These patients comprise a diverse and heterogeneous group usually excluded from surgery due to advanced tumour stage or the presence of concomitant extrahepatic disease. To date, no randomized clinical trial on the surgical treatment of NCRLM has been conducted, and only few retrospective reports are available.The scope of this research project is to develop a large registry of patients undergoing liver surgery for non-colorectal liver metastases.

Criteria for eligibility:

Study pop:
All patients with a diagnosis, based on imaging methods and histologically confirmed, of NCRLM, consecutively referred to centres with expertise in hepatobiliary surgery will be evaluated for inclusion. For the diagnosis and staging of disease the participating centres will refer to the guidelines for NCRLM, together with the established clinical habits present in each centre

Sampling method: Non-Probability Sample
Criteria:
Inclusion criteria: - Signature informed consent - Age ≥ 18 years - Histologically confirmed diagnosis of NCRLM (first diagnosis or relapse) - Liver resection performed. Exclusion criteria - ASA IV - Severe psychiatric pathology - Unable to follow a clinical examination pattern during observation. - Patient submitted exclusively to interventional locoregional procedures other than liver resection.

Gender: All

Minimum age: 18 Years

Maximum age: N/A

Healthy volunteers: No

Start date: January 1, 2025

Completion date: June 30, 2029

Lead sponsor:
Agency: Azienda Ospedaliero Universitaria Maggiore della Carita
Agency class: Other

Source: Azienda Ospedaliero Universitaria Maggiore della Carita

Record processing date: ClinicalTrials.gov processed this data on November 12, 2024

Source: ClinicalTrials.gov page: https://clinicaltrials.gov/ct2/show/NCT06542926

Login to your account

Did you forget your password?