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Clinical Trial Summary

A multicentre phase II study to determine the safety and efficacy of EUS-guided nCLE in patients with suspected cystic tumours of the pancreas in whom endoscopic ultrasound-guided fine needle aspiration (EUS-FNA) is clinically indicated. Patients will be recruited sequentially to undergo nCLE as part of their routine diagnostic evaluation, followed by standard surveillance. This part of the study will recruit 60 patients.


Clinical Trial Description

A multicentre phase II study to determine the safety and efficacy of EUS-guided nCLE in patients with suspected cystic tumours of the pancreas in whom endoscopic ultrasound-guided fine needle aspiration (EUS-FNA) is clinically indicated. Patients will be recruited sequentially to undergo nCLE as part of their routine diagnostic evaluation, followed by standard surveillance. This part of the study will recruit 60 patients. The study also includes a feasibility study to evaluate the role of intraoperative nCLE in the diagnosis and staging of pancreatic tumours. This part of the study will recruit a further 20 patients.

Primary endpoint:

Assess the diagnostic performance of the Cellvizio nCLE system in the characterization of pancreatic cysts, compared to standard diagnostic modalities.

Secondary endpoints:

- Assess the safety and efficacy of EUS-nCLE.

- Assess the impact of the Cellvizio nCLE system on the management of patients with pancreatic cysts.

- Develop and validate interpretation criteria for nCLE in the pancreas.

- Assess the diagnostic performance of nCLE in characterising and staging pancreatic tumours intraoperatively. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02523170
Study type Interventional
Source University College, London
Contact
Status Completed
Phase N/A
Start date July 2014
Completion date April 2018

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