US-nCLE: Clinical Registry of nCLE in Masses and Cystic Tumors of the Pancreas, Lymph Nodes, Submucosal Lesions of the GI Tract

Sponsor
Mauna Kea Technologies (Industry)
Overall Status
Completed
CT.gov ID
NCT01770405
Collaborator
(none)
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Study Details

Study Description

Brief Summary

This study focuses on four different lesions: pancreatic cysts, lymph nodes near the gastrointestinal tract, pancreatic masses and GIST tumors.

On one hand, the results obtained during previous studies are more advanced for the assessment of the diagnostic performance of Cellvizio needle-based Confocal Laser Endomicroscopy (nCLE) system for Pancreatic cysts. Safety and technical feasibility have already been performed, and an interpretation criteria classification exists. On the other hand, results for pancreatic masses, Lymph nodes and GIST are less developed.

the objectives of the study are to

  • Assess the diagnostic performance of the Cellvizio needle-based Confocal Laser Endomicroscopy (nCLE) system in diagnosing masses and cystic tumors of the pancreas, lymph nodes, submucosal lesions of the GI tract

  • Define/Validate descriptive criteria of nCLE sequences in masses and cystic tu-mors of the pancreas, lymph nodes, submucosal lesions of the GI tract

Condition or Disease Intervention/Treatment Phase
  • Device: Endoscopic ultrasound fine needle aspiration

Detailed Description

The principle of needle-based Confocal Laser Endomicroscopy (nCLE) is to image organs within or adjacent to the GI or respiratory tracts by means of a miniprobe inserted through an endoscopic needle. The fundamental technology, as well as the principle of operation of nCLE, is substantially similar to pCLE.

endoscopic fine needles are used during EUS-FNA procedures to puncture solid organs such as the pancreas, in order to get tissue or fluid for diagnostic purposes. There are different calibers of endoscopic nee-dles used. The most commonly used calibers for EUS-FNA procedures are 22G, 19G, and 25G needles. The nCLE Confocal Miniprobe is compatible with the 19G-type needle only. It is expected to help to differentiate the different types of lesions, especially for cysts, leading to better patient management. Microscopic tissue information in real-time in vivo during an EUS-FNA procedure may allow better differentiation between mucinous and non-mucinous cysts for instance.

Study Design

Study Type:
Observational [Patient Registry]
Actual Enrollment :
40 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Registry Trial for Clinical Evaluation of nCLE in Masses and Cystic Tumors of the Pancreas, Lymph Nodes, Submucosal Lesions of the GI Tract
Study Start Date :
Sep 1, 2013
Actual Primary Completion Date :
Dec 21, 2016
Actual Study Completion Date :
Dec 21, 2016

Arms and Interventions

Arm Intervention/Treatment
pancreatic cysts

Patient indicated for a first endoscopic ultrasound fine needle aspiration (EUS-FNA) for a pancreatic cyst,

Device: Endoscopic ultrasound fine needle aspiration
Device: nCLE needle-based Confocal Laser Endomicroscopy
Other Names:
  • ultrasonographic endoscopy
  • EUS-guided FNA
  • Outcome Measures

    Primary Outcome Measures

    1. performance evaluation [up to one year]

      Assess the diagnostic performance of the Cellvizio needle-based Confocal Laser Endomicroscopy (nCLE) system in diagnosing masses and cystic tumors of the pancreas, lymph nodes, submucosal lesions of the GI tract (accuracy evaluation) Define/Validate descriptive criteria for nCLE sequences in the characterization of masses and cystic tumors of the pancreas, lymph nodes, submucosal lesions of the GI tract (image interpretation criteria definition

    Secondary Outcome Measures

    1. Safety and feasibility evaluation [up to one month following the procedure]

      Evaluate the feasibility and safety of nCLE for the characterization of masses and cystic tumors of the pan-creas, lymph nodes, submucosal lesions of the GI tract (IE. number of patients with complications, number of adverse events) Build an atlas of images of nCLE sequences of masses and cystic tumors of the pancreas, lymph nodes, submucosal lesions of the GI tract

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
      • Male or female > 18 years of age
    • Patient indicated for a first EUS-FNA for masses and cystic tumors of the pancreas, lymph nodes, submu-cosal lesions of the GI tract

    • Patients who had previous non-diagnostic tissue sampling taken during a previous EUS-FNA for masses and cystic tumors of the pancreas, lymph nodes, submucosal lesions of the GI tract

    • Patient with known masses and cystic tumors of the pancreas, lymph nodes, submucosal lesions of the GI tract

    • For pancreatic cyst patient, suffering chronic calcifying pancreatitis

    • For pancreatic mass patient, any size or location

    • For lymph node patient, any node reachable with EUS-FNA

    • Willing and able to comply with study procedures and provide written informed consent to participate in the registry

    Exclusion Criteria:
      • Subjects for whom EUS-FNA procedures are contraindicated
    • Known allergy to fluorescein contrast

    • If female, breast feeding or pregnant based on a positive hCG serum or an in vitro diagnostic test result

    • Subject with multiple cysts

    • Cysts <20 mm in diameter

    • Previous EUS-FNA procedure performed less than 3 months ago

    • If several pancreatic masses, only one will be imaged during the nCLE procedure

    • Lymph nodes <5 mm in diameter

    • If several suspicious lymph nodes, only the most suspect will be imaged during the nCLE proce-dure

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Emory University Hospital Atlanta Georgia United States 30322
    2 North Shore-LIJ Health System Manhasset New York United States 11030
    3 Columbia University Medical Center New York New York United States 10032
    4 Temple University Hospital Philadelphia Pennsylvania United States 19140

    Sponsors and Collaborators

    • Mauna Kea Technologies

    Investigators

    • Principal Investigator: Divyesh V Sejpal, MD, Northwell Health

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Mauna Kea Technologies
    ClinicalTrials.gov Identifier:
    NCT01770405
    Other Study ID Numbers:
    • MKT_2012_nCLE_03
    First Posted:
    Jan 17, 2013
    Last Update Posted:
    Aug 29, 2017
    Last Verified:
    Aug 1, 2017
    Keywords provided by Mauna Kea Technologies
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Aug 29, 2017