NCT03616860Befejeződött
Assessment of Safety and Feasibility of ExAblate Blood-Brain Barrier (BBB) Disruption for Treatment of Glioma
Assessment of Safety and Feasibility of ExAblate Blood-Brain Barrier Disruption for the Treatment of High Grade Glioma in Patients Undergoing Standard Chemotherapy
Forrás: ClinicalTrials.gov · Utoljára frissítve: 2024. jan. 23.
Rövid összefoglaló (regiszter, angolul)
The purpose of this study is to evaluate the safety of blood-brain barrier (BBB) disruption in adult patients with a first presentation of a glioblastoma (GBM) following a maximal safe surgical resection and standard chemo-radiation with temozolomide (TMZ) protocol and ready for the maintenance phase of the Stupp protocol with TMZ.
- Állapot (regiszter)
- Befejeződött
- Vizsgálattípus
- Beavatkozással járó
- Résztvevők száma
- 14 (tényleges)
- Első benyújtás
- 2018. júl. 20.
- Kezdés
- 2018. okt. 16.
- Elsődleges befejezés
- 2023. dec. 31.
- Fő szponzor
- InSightec
- Betegségek
- Glioblasztóma
- NCT-szám
- NCT03616860
Mit vállalsz
- Vizsgálat típusa: Beavatkozással járó
- Bevont résztvevők: 14
- 2018. okt. 16. és az elsődleges befejezés (2023. dec. 31.) között
- 1 helyszín, 1 országban
- Vizitek és vizsgálatok: kérdezd a vizsgálat csapatát, a regiszter nem sorolja fel őket
A(z) ClinicalTrials.gov regisztermezőiből összeállítva. A vizsgálat felépítését írja le.
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Korábbi kezelés
- The sonication pathway to the tumour involves:
- Extensive scalp scars, ii. Clips or other metallic implanted objects in the skull or the brain (brain implants).
- Patients requiring increasing doses of corticosteroids.
- Patient receiving bevacizumab (Avastin) therapy.
- Patients undergoing other concurrent therapies such as chemotherapy wafers, immunotoxins delivered by convection-enhanced delivery, regionally administered gene and viral therapies, immunotherapies, and focal irradiation with brachytherapy, stereotactic radiosurgery, and laser interstitial thermotherapy.
- Anti-coagulant therapy, or medications known to increase risk of hemorrhage within washout period prior to treatment.
- Previous full course of chemotherapy.
Más betegség
- Patients presenting with the following imaging characteristics:
- Evidence of recent intracranial hemorrhage.
- Severe hypertension (diastolic BP > 100 on medication).
- History of a bleeding disorder, coagulopathy or with a history of spontaneous tumour hemorrhage.
- Insulin-dependent diabetes mellitus that is not well-controlled or that in the Investigator's opinion precludes participation in the study.
- Known life-threatening systemic disease.
- Cardiac shunt.
- Allergy to eggs or egg products.
- Subjects with evidence of cranial or systemic infection.
- Subjects with chronic pulmonary disorders.
- Subjects with a history of drug allergies, asthma or hay fever, and multiple allergies, in particular subjects with a history of anaphylaxis.
- Subjects with evidence of Hepatitis B virus infection/carrier state.
Laborértékek
- Cardiac disease or unstable hemodynamics including:
- Documented myocardial infarction within six months of enrollment. ii. Unstable angina on medication. iii. Congestive heart failure. iv. Left ventricular ejection fraction <50%. v. History of a hemodynamically unstable cardiac arrhythmia. vi. Cardiac pacemaker.
Egyéb
- The subject presents with symptoms and signs of increased intracranial pressure (e.g., headache, nausea, vomiting, lethargy, and papilledema).
- Documented cerebral infarction within the past 12 months.
- TIA in the last 1 month.
- Cerebral or systemic vasculopathy.
- Known sensitivity to gadolinium-DTPA.
- Known sensitivity to DEFINITY ultrasound contrast agent or perflutren.
- Contraindications to MRI such as non-MRI-compatible implanted devices.
- Large subjects not fitting comfortably into the MRI scanner.
- Difficulty lying supine and still for up to 4 hours in the MRI unit or claustrophobia.
- Untreated, uncontrolled sleep apnea.
- Positive pregnancy test (for pre-menopausal women).
- Severely impaired renal function.
- Liver injury as indicated by liver function tests.
Kiket keres a vizsgálat
- Men or women.
- Age between 18 and 80 years, inclusive.
- Able and willing to give informed consent.
- Grade IV malignant glioma (GBM) confirmed through assessment of surgical specimens by a board-certified neuropathologist.
- Undergone maximal safe surgical resection and completed concurrent radiotherapy+oral TMZ without any complications and deemed eligible for the maintenance phase of TMZ treatment.
- Karnofsky rating 70-100.
- ASA score 1-3.
- Able to communicate during the ExAblate MRgFUS procedure.
- Able to attend all study visits (i.e., life expectancy of at least 3 months).
Életkor a regiszterben: 18 év – 80 év · Nem: nők és férfiak · Egészséges önkénteseket nem fogad
Helyszínek (1)
Helyszínek a regiszter sorrendjében. Ha a profilodba mented a városodat, távolság szerint rendeződnek.
| Helyszín | Város | Ország | Helyszín állapota |
|---|---|---|---|
| Sunnybrook Health Sciences Centre | Toronto | Kanada | Ismeretlen állapot |
Kapcsolódó publikációk
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