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Clinical Trial Details — Status: Enrolling by invitation

Administrative data

NCT number NCT01073358
Other study ID # NNR-5
Secondary ID
Status Enrolling by invitation
Phase N/A
First received February 22, 2010
Last updated October 26, 2017
Start date March 9, 2010
Est. completion date December 2021

Study information

Verified date October 2017
Source Heidelberg University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

It is uncertain, whether hilar lymphadenectomy should be performed routinely in patients undergoing resection of colorectal liver metastases.

For this reason it is the aim of the present prospective randomized trial to evaluate, if routine lymphadenectomy reduces recurrent disease in patients undergoing resection of colorectal liver metastases.


Description:

Routine lymphadenectomy in patients undergoing hepatic resection for colorectal liver metastases may improve outcome of further patients due to the presence of micrometastases that have been shown to be of prognostic relevance. While previous studies highlight the clinical significance of perihepatic lymph node metastases, the outcome of patients with and without hilar lymphadenectomy has not yet been compared and thus no clear conclusion about the clinical value of routine hilar lymphadenectomy in CRC patients undergoing resection of liver metastases can be drawn from present data.

As disease recurrence occurs frequently and may affect up to 75 % of patients, further strategies are required to improve postoperative outcome. Routine hilar lymphadenectomy may offer an effective approach to remove residual disease and by this to reduce disease recurrence with little additional morbidity. For this reason it is the aim of the present prospective randomized trial to evaluate, if routine lymphadenectomy reduces recurrent disease in patients undergoing resection of colorectal liver metastases.


Recruitment information / eligibility

Status Enrolling by invitation
Enrollment 166
Est. completion date December 2021
Est. primary completion date July 2019
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Patients scheduled for curative (R0) resection

- No evidence of extrahepatic disease

- No history of previous hepatic lymphadenectomy

- Age equal or greater than 18 years

- Written Informed consent

Exclusion Criteria:

- Expected lack of compliance

- Impaired mental state or language problems

- History of another primary cancer, except:

- Curatively treated in situ cervical cancer or curatively resected non-melanoma skin cancer

- Other primary solid tumour curatively treated with no known active disease present and no treatment administered for = 5 years prior to randomisation

Study Design


Intervention

Procedure:
Routine hilar lymphadenectomy
Hilar lymphadenectomy is performed before actual resection of the colorectal liver metastases

Locations

Country Name City State
Germany Department of Gastrointestinal, Thoracic and Vascular Surgery Dresden

Sponsors (1)

Lead Sponsor Collaborator
Heidelberg University

Country where clinical trial is conducted

Germany, 

Outcome

Type Measure Description Time frame Safety issue
Primary rate of disease recurrence 2 years after surgery
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