FLUOGOD: Intraoperative Fluorescence of Ganglogliomas and Neuroepithelial Dysembryoplastic Tumors

Sponsor
Rennes University Hospital (Other)
Overall Status
Completed
CT.gov ID
NCT03970785
Collaborator
(none)
7
1
10
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Study Details

Study Description

Brief Summary

One of the key issues of tumour brain surgeries is to clearly define the borders of the tumor. The investigators proposed to evaluate the feasibility of intraoperative fluorescein guidance. Patients will be identified from the list of patients operated on under fluorescence to collect clinical datas. Surgical videos will be analyzed to assess the presence of intraoperative fluorescence and its subjectively judged intensity. MRI data will be extracted from the radiological reports to assess quality extraction. No additional data will be produced

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    Gangliogliomas typically present as a slow-growing, cystic mass taking contrast, while dysembryoplastic neuro-epithelial tumors commonly show microcystic patterns, inconstant contrast-enhancement and are preferentially located on the internal face of the temporal lobe. The cornerstone of the treatment of these two entities remains surgery, as it provides good oncological outcomes and control of seizures. Surgical resection keeps a major role for these tumors. Thus, one of the key issues is to clearly define the borders of the tumor during surgery, a point of considerable importance for these curable lesions. Then, the investigators proposed to evaluate the feasibility of intraoperative fluorescein guidance, a technique based on the staining of blood-brain barrier breakdown areas with fluorescein. Patients will be identified from the list of patients operated on under fluorescence maintained by the department since the acquisition of the technique. Clinical datas will be collected and surgical videos will be analyzed to assess the presence of intraoperative fluorescence and its subjectively judged intensity (absent, weak, medium, strong). MRI data (quality of excision: total, subtotal or partial according to usual criteria) will be extracted from the radiological reports. No additional data will be produced

    Study Design

    Study Type:
    Observational
    Actual Enrollment :
    7 participants
    Observational Model:
    Case-Only
    Time Perspective:
    Retrospective
    Official Title:
    Intraoperative Fluorescence of Gangliogliomas and Neuroepithelial Dysembryoplastic Tumors
    Actual Study Start Date :
    Jul 15, 2018
    Actual Primary Completion Date :
    Apr 30, 2019
    Actual Study Completion Date :
    May 15, 2019

    Outcome Measures

    Primary Outcome Measures

    1. Number of Intraoperative tumor fluorescence [2 months]

      Number of patients which present intraoperative tumor fluorescence. Fluorescence will be assessed using surgical videos.

    Secondary Outcome Measures

    1. Number of allergic events [2 months]

      Number of allergic events during fluorescein-based surgery

    2. Percentage of excised tumour volume [2 months]

      Percentage of excised tumour volume. Quality of excision on the post-operative MRI control according to the volume of the remaining pathological contrast intake (complete, subtotal or partial)

    3. Number of epilepsy events after surgery [2 months]

      Occurence of postoperative epilepsy events using Engels classification. (Class I: Free of disabling seizures, Class II: Rare disabling seizures ("almost seizure-free"), Class III: Worthwhile improvement, Class IV: No worthwhile improvement)

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Over 18 years old patient

    • Fluoroguided removal of a histologically proven Ganglioglioma or Dysembryoplastic Neuroepithelial Tumors between 2015-2018

    • Surgical video available

    Exclusion Criteria:
    • Absence of surgical video

    • Adults who are subject to legal protection (protection of justice, guardianship, guardianship)

    • Patient objecting to the use of their data

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 CHU Rennes Rennes France

    Sponsors and Collaborators

    • Rennes University Hospital

    Investigators

    • Principal Investigator: Pierre-Jean LE RESTE, Md, Rennes University Hospital

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Rennes University Hospital
    ClinicalTrials.gov Identifier:
    NCT03970785
    Other Study ID Numbers:
    • 35RC18_3046_FLUOGOD
    First Posted:
    Jun 3, 2019
    Last Update Posted:
    Jun 4, 2019
    Last Verified:
    May 1, 2019
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by Rennes University Hospital
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Jun 4, 2019