NCT07224451 Liquid Biopsy Following BBB Disruption Using Barrier Disrupting Fields in Patients Undergoing Spine Surgery
| NCT ID | NCT07224451 |
| Status | Recruiting |
| Phase | — |
| Sponsor | Sheba Medical Center |
| Condition | Spinal Tumors |
| Study Type | INTERVENTIONAL |
| Enrollment | 20 participants |
| Start Date | 2025-10-16 |
| Primary Completion | 2027-10 |
Eligibility & Interventions
Eligibility Fast-Check
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What to Expect as a Participant
You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.
This trial targets 20 participants in total. It began in 2025-10-16 with a primary completion date of 2027-10.
⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.
Brief Summary
Objective: To identify new central nervous system (CNS) biomarkers to be used for blood-derived liquid biopsy once the blood-brain barrier (BBB), specifically the blood-arachnoid barrier (BAB), has been transiently disrupted by BDF in patients undergoing spine surgery. Design: Single center (Sheba Medical Center), prospective, controlled. Phase: Feasibility study Endpoints: Efficacy The primary endpoint of the study is the elevation in blood concentration of CNS biomarkers following the study procedure compared to biomarkers detected in cerebrospinal fluid (CSF) of the same subject. Safety The primary safety endpoint will be the overall incidence of BDF procedure-related AEs and SAEs, with severity graded according to CTCAE v5.0 criteria. Study population: The study population will include up to 20 patients undergoing spine surgery. Study period: 24 months. Inclusion criteria: 1. Adult subjects over the age of 18 2. Able to sign informed consent 3. Candidates for intradural tumor resection spinal surgery with intraoperative neuromonitoring. Exclusion criteria: 1. Pacemakers, or other implanted electric medical devices 2. Pregnant or lactating females 3. Major medical, neurologic or psychiatric condition who are judged as unable to fully comply with the study 4. History of skull fractures or previous brain surgery 5. American Society of Anesthesiologists grade \>2 6. Anticoagulants treatment 7. Damage to the dura resulting in CSF leak 8. Patients with seizures/epilepsy Study procedure: 1. Candidates for intradural tumor resection spinal surgery with intraoperative neuromonitoring will be enrolled in the study prior to surgery. 2. The patient will undergo preparation for surgery according to the standard care. 3. Once anesthetized and intubated, electrodes will be attached to the patient's head. 4. After placing the electrodes, when the patient is under anesthesia, a blood sample will be taken prior to BDF. This sample will be used as baseline for BDF. 5. The patient will then undergo a BDF procedure. 6. Additional blood samples will be taken for identification of CNS biomarkers. 7. Surgery will then proceed according to the standard of care. 8. Once the dura is opened, a CSF sample will be taken, in order to compare the blood biomarkers of the specific subject with the CSF biomarkers. 9. The surgery will continue according to the standard of care.
Eligibility Criteria
Inclusion Criteria: * Adult subjects over the age of 18 * Able to sign informed consent * Candidates for intradural tumor resection spinal surgery with intraoperative neuromonitoring. Exclusion Criteria: * Pacemakers, or other implanted electric medical devices * Pregnant or lactating females * Major medical, neurologic or psychiatric condition who are judged as unable to fully comply with the study * History of skull fractures or previous brain surgery * American Society of Anesthesiologists grade \>2 * Anticoagulants treatment * Damage to the dura resulting in CSF leak * Patients with seizures/epilepsy
Contact & Investigator
Ran Harel, MD
PRINCIPAL INVESTIGATOR
Sheba Medical Center
Frequently Asked Questions
Who can join the NCT07224451 clinical trial?
This trial is open to participants of all sexes, aged 18 Years or older, studying Spinal Tumors. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.
Is NCT07224451 currently recruiting?
Yes, NCT07224451 is actively recruiting participants. Contact the research team at yael.mardor@sheba.health.gov.il, yael.mardor@gmail.com for enrollment information.
Where is the NCT07224451 trial being conducted?
This trial is being conducted at Ramat Gan, Israel.
Who is sponsoring the NCT07224451 clinical trial?
NCT07224451 is sponsored by Sheba Medical Center. The principal investigator is Ran Harel, MD at Sheba Medical Center. The trial plans to enroll 20 participants.