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Clinical Trials in Germany / NCT07021573
Starting soon Not applicable

Protoporphyrin Imaging in Multispectral Evaluation of Resections

NCT07021573 · tracked via the Priya Life Science Germany tracker
Phase
Not applicable
Started
2025-09-30
Last updated
2025-09-09

Condition(s) studied

Glioma

Investigational drug(s) / intervention(s)

KINEVO 900 S with BLUE 400

KINEVO 900 S with BLUE 400: The investigational device consists of a CE marked (MDR) surgical microscope KINEVO 900 S by Carl Zeiss Meditec AG, including the BLUE 400 fluorescence option. This microscope is equipped with an additional component (CALLAO), provided by the Carl Zeiss Meditec AG, that allows for extended, multispectral, image acquisition in the operating room. CALLAO consists of an optical setup with additional cameras, that can be mounted on the main system KINEVO 900 S, and a second light source for specific illumination during image acquisition with the CALLAO cameras.

Study summary

Observational non-interventional investigation to evaluate the potential of multispectral imaging in improving tumor visualization.

Eligibility

Sex
ALL
Min age
18 Years
Max age
99 Years
Healthy volunteers
No
Inclusion criteria: * Age Requirement: Patients must be 18 years of age or older. * Diagnosis: Patients with a preoperative diagnosis of a suspected high-grade glioma based demographics and MRI imaging. * MRI Findings: Patients must meet one of the following criteria: * Group 1: Suspected high-grade glioma with contrast enhancement on MRI (GBM-like). * Group 2: Suspected high-grade glioma without contrast enhancement on MRI (LGG-like). * Surgical Resection: Patients scheduled to undergo surgical resection of the tumor as part of standard treatment. * 5-ALA Administration: Patients who will receive 5-aminolevulinic acid (5-ALA) for fluorescence guidance during surgery. * Post-op MRI: Patients who are able to undergo pre- and postoperative MRI (standard of care at the center). * Informed Consent: Patients who are able to understand and provide written informed consent prior to enrollment in the study. * Eligibility for Multispectral Imaging: Patients whose surgical procedures allow for the use of multispectral imaging technology for tumor visualization. * Performance Status: Patients with a Karnofsky Performance Status (KPS) of 60 or greater, indicating that they are capable of at least limited self-care. * No Prior Treatment: Patients who have not received prior treatment for the current brain tumor, including surgery, radiotherapy, or chemotherapy. Exclusion criteria: * Patients with a known allergy or contraindication to 5-aminolevulinic acid (5-ALA) or its components. * Use of all other fluorescent markers. * Patients with a history of porphyria or other disorders related to 5-ALA metabolism. * Patients with recurrent gliomas or those who have received prior treatment for their current brain tumor, including surgery, radiotherapy, or chemotherapy. * Pregnant or breastfeeding patients, due to potential risks associated with 5-ALA administration. * Patients with severe comorbidities or other medical conditions that, in the investigator's opinion, would pose an unacceptable risk or compromise the safety of participation in the study. * Patients with a Karnofsky Performance Status (KPS) below 60, indicating an inability to perform minimal self-care. * Patients with a history of severe hepatic or renal impairment that may impact the metabolism of 5-ALA. * Patients unable to undergo MRI imaging for any reason (e.g., presence of non-MRI-compatible implants). * Patients unable to provide written informed consent due to cognitive, language, or other barriers. * Patients with tumors located in regions where fluorescence imaging is not technically feasible or where the use of multispectral imaging could interfere with the standard surgical approach. * Pregnancy

Primary outcome measure(s)

Trial sites (10)

FacilityCityRegionStatus
Universitätsklinik für Neurochirurgie der Medizinischen Universität Innsbruck Innsbruck Austria
Charité - Universitätsmedizin Berlin Berlin Germany
Universitätsklinikum Freiburg - Klinik für Neurochirurgie im Neurozentrum Freiburg im Breisgau Germany
Universitätsklinikum Göttingen - Neurochirurgische Klinik Göttingen Germany
Klinik und Poliklinik für Neurochirurgie, LMU Klinikum München München Germany
Klinikum rechts der Isar der Technischen Universität München München Germany
Universitätsklinikum Münster - Klinik für Neurochirurgie Münster Germany
Universitätsklinikum Tübingen, Universitätsklinik für Neurochirurgie Tübingen Germany
Inselspital Bern, Universitätsklinik für Neurochirurgie Bern Switzerland
Hôpitaux universitaires de Genève - NeuroCentre Geneva Switzerland

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07021573 on ClinicalTrials.gov ↗ ← All trials in Germany