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Sentinel Node in Colon Cancer


Trial Overview

StatusConditionSponsor/Collaborator(s)First ReceivedLast ChangedVerification Date
Recruiting Colon Cancer University Hospital, Strasbourg, France Other December 12, 2006 January 9, 2009 January 2009

Study TypeStudy DesignPhaseEnrollmentStart DateEnd Date
Interventional Allocation: Non-Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Diagnostic N/A 140 March 2007 -

Locations

FacilityAddressContactPhoneEmailStatus
Service de Chirurgie Générale et Digestive - Hôpital de Hautepierre Strasbourg 67098 France Cécile Brigand, MD - cecile.brigand@chru-strasbourg.fr Recruiting

Intervention

TypeInterventionDescription
Procedure blue and isotopic detection of sentinel lymph nodes -

Outcome

TypeMeasureTime FrameSafety Issue
Primary Survival without recurrence after 3 years - -

Official Title

Sentinel Node Study in Colon Cancer Surgery

Eligibility

GenderMinimum AgeMaximum AgeHealthy Volunteers
Both - N/A No

Inclusion Criteria:

- adult

- colon cancer

- open surgery

Exclusion Criteria:

- emergency surgery

- metastases