Clinical Trials Directory

Trials / Completed

CompletedNCT02151097

PRIME - PRostate Imaging for Margin Evaluation

A Feasibility Study to Evaluate 18F-choline Cerenkov Luminescence Imaging for Measuring Margin Status in Radical Prostatectomy Specimens

Status
Completed
Phase
Study type
Observational
Enrollment
7 (actual)
Sponsor
Lightpoint Medical Limited · Industry
Sex
Male
Age
18 Years
Healthy volunteers
Not accepted

Summary

This study will evaluate the feasibility of using intra-operative Cerenkov Luminescence Imaging (CLI) of prostatectomy specimens to determine tumour margin status. The samples will be imaged using the LightPathTM Imaging System which consists of a light-tight box containing an ultra-sensitive lens and radiation-shielded camera. This study will measure the correlation between margin status of the WLE specimen and the metastatic status of dissected lymph nodes as determined by the LightPathTM Imaging System and by histopathology. This is a pilot study to assess feasibility before proceeding to a pivotal study to evaluate the benefits of the LightPathTM system in clinical practice.

Detailed description

This study is a prospective, single-centre feasibility study to evaluate the use of intra-operative Cerenkov Luminescence Imaging (CLI) of prostatectomy specimens to determine margin status. Subjects will receive an intravenous injection of 370 Mega Becquerel (MBq) of 18F-choline prior to routine, elective radical prostatectomy. The surgery will be performed according to standard-of-care. The resected prostatectomy specimens will be imaged using the LightPathTM Imaging System, consisting of a light-tight box containing an ultra-sensitive lens and Electron Multiplying Charged-Coupled Device (EMCCD) camera. This study will measure the agreement between margin status of the prostatectomy specimen as determined by CLI and by histopathology (reference method). This study will assess feasibility before proceeding to a pivotal study to evaluate the benefits of the LightPathTM Imaging System in clinical practice.

Conditions

Timeline

Start date
2014-11-01
Primary completion
2016-06-01
Completion
2016-06-01
First posted
2014-05-30
Last updated
2016-06-23

Locations

1 site across 1 country: United Kingdom

Source: ClinicalTrials.gov record NCT02151097. Inclusion in this directory is not an endorsement.