Clinical Trials Directory

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UnknownNCT02403050

Feasibility Study of Fiducial Markers in Oesophageal Cancer

Feasibility Study to Assess the Benefit of Using Fiducial Markers for Patients Receiving Radiotherapy for Cancer of the Oesophagus

Status
Unknown
Phase
Study type
Observational
Enrollment
40 (estimated)
Sponsor
NHS Greater Glasgow and Clyde · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

Currently, patients of suitable fitness with non-metastatic esophageal cancer are treated with surgery, radiotherapy or chemoradiotherapy. If treated with radio or chemoradiotherapy, a Computerised tomography (CT) scan is performed and is the dataset used for planning radiotherapy. Information from the endoscopic ultrasound (EUS), performed during routine staging, is used to help localize the tumor, as tumors of the esophagus are poorly visualised on CT. This information is subjective and dependant on the clinician performing the procedure. The tumor is described in relation to common anatomical landmarks. Interpretion of this information can lead to over-compensation when attempting to cover the tumor with a radiation field, to avoid a "miss". It is thought that using fiducial markers called Visicoils placed in or adjacent to the tumor's top and bottom extent at the time of EUS, will lead to better definition of the tumor in the planning process and hence, improvement in local tumor control, and reduction in radiotherapy dose to normal tissue.

Conditions

Interventions

TypeNameDescription
DEVICEFiducial markers2 fiducial markers (Visicoils) to be placed in the tumor area

Timeline

Start date
2015-03-01
Primary completion
2019-03-01
Completion
2019-03-01
First posted
2015-03-31
Last updated
2015-03-31

Locations

1 site across 1 country: United Kingdom

Source: ClinicalTrials.gov record NCT02403050. Inclusion in this directory is not an endorsement.