Bone Tumor Clinical Trial
Official title:
Assessment of Operative Time, Precision, and Safety of an Augmented Reality Navigation System (Endosight) for the Guidance of Bone Biopsy
NCT number | NCT05732558 |
Other study ID # | ESBB1 |
Secondary ID | |
Status | Completed |
Phase | N/A |
First received | |
Last updated | |
Start date | December 16, 2022 |
Est. completion date | March 8, 2023 |
Verified date | March 2023 |
Source | R.A.W. - S.R.L. |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The goal of this clinical study is to evaluate the duration of the procedure, the precision (distance between the needle tip and the centre of the target), and the safety of endosight system in the guidance for bone biopsies.
Status | Completed |
Enrollment | 16 |
Est. completion date | March 8, 2023 |
Est. primary completion date | March 8, 2023 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: - Patient with a bone lesion for which a percutaneous biopsy is indicated; - Informed consent signed by the patient for participation in the study. Exclusion Criteria: - Age < 18 years; - Pregnant and lactating women (assessed through auto declaration of the patient) |
Country | Name | City | State |
---|---|---|---|
Italy | IRCCS Ospedale Galeazzi - Sant'Ambrogio | Milano | MI |
Lead Sponsor | Collaborator |
---|---|
R.A.W. - S.R.L. |
Italy,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Procedure time | Change in the total duration of the procedure (calculated from the time of local anesthesia injection to the time of bone sample collection) | During bone biopsy procedure (after the bone sample has been collected) | |
Primary | Total number of CT-SCAN | Change in overall number of CT scans performed during the procedure (calculated as the total number of CT scans required to reach the target; from the 1° CT-scan (local anesthesia) to the last CT-scan (sample collection from the bone) | During bone biopsy procedure (after the bone sample has been collected) | |
Secondary | endosight accuracy | Distance between the tip of the needle and the center of the target (from 0mm to 10mm) | During bone biopsy procedure (after the bone sample has been collected) | |
Secondary | Total radiation dose | Change in the total radiant dose received by the patient (calculated by summing the radiation emitted for each CT-Scan performed from the anesthesia-point to the collection-point) | During bone biopsy procedure (after the bone sample has been collected) | |
Secondary | Operator satisfaction | satisfaction level of the operator (from 0 to 5 - 1: poor satisfaction, 5: high satisfaction) | During bone biopsy procedure (after the bone sample has been collected) | |
Secondary | Side effects | Total number of major+minor side effects, reported during the procedure | During bone biopsy procedure (after the bone sample has been collected) |
Status | Clinical Trial | Phase | |
---|---|---|---|
Not yet recruiting |
NCT05515068 -
Registry For Children, Adolescents And Adults With Osteosarcoma And Biologically Related Bone Sarcomas
|
||
Completed |
NCT02862288 -
Preliminary Study of Microwave Tumoral Ablation Performances for the Treatment of Pulmonary, Renal and Bone Neoplasia.
|
Phase 1/Phase 2 | |
Withdrawn |
NCT01679691 -
The Epidural Anesthesia on the Intra-operative and Post-operative Amount of Bleeding Post Lower Limb Salvage Surgery
|
N/A | |
Recruiting |
NCT04178044 -
Phase Ⅰ Clinical Study Protocol of GB223 Monoclonal Antibody Injection
|
Phase 1 | |
Completed |
NCT03389724 -
Prevention of Chemotherapy Induced Cardiotoxicity in Children With Bone Tumors and Acute Myeloid Leukemia
|
Phase 3 | |
Completed |
NCT05075889 -
Utility of ICG in Benign Bone Tumors
|
Early Phase 1 | |
Completed |
NCT04755140 -
Endoprosthesis Metal Toxicity Study
|
||
Not yet recruiting |
NCT03427632 -
Role of Percutaneous Vertebroplasty in Treatment of Vertebral Tumors
|
N/A | |
Completed |
NCT04798326 -
Comparing of the Pharmacokinetic, Pharmacodynamic, Safety and Immunogenicity of MW032 and Xgeva® in Healthy Adults
|
Phase 1 | |
Recruiting |
NCT06459141 -
The Effect of Hemodilution on Intraoperative Allogeneic Transfusion (HEAL)
|
N/A | |
Not yet recruiting |
NCT06453642 -
Evaluation of a Simple-Prep Controlled Embolic
|
N/A | |
Active, not recruiting |
NCT04104750 -
The Assessment of Fatigue and Quality of Life in Patients With Bone Tumor,
|
||
Completed |
NCT00598741 -
Dynamic Contrast Enhanced MRI(DCE-MRI)of Bone Tumors
|
N/A | |
Completed |
NCT02398058 -
Trabectedin Plus Olaparib in Metastatic or Advanced Sarcomas (TOMAS)
|
Phase 1 | |
Recruiting |
NCT06171282 -
A Clinical Study on Oncolytic Virus Injection (R130) for the Treatment of Advanced Bone and Soft Tissue Tumors
|
Early Phase 1 | |
Not yet recruiting |
NCT06376682 -
EPIBONE Study: a Prospective Study on Feasibility, Safety and Accuracy
|
N/A | |
Enrolling by invitation |
NCT05772312 -
Quality of Life of Patients With Bone Tumor of the Lower Limbs Treated With Salvage Surgery
|
||
Recruiting |
NCT06455722 -
[68Ga]Ga-P15-041 PET/CT in Variety of Bone Tumors
|
Early Phase 1 | |
Recruiting |
NCT05779670 -
Adherence to a Personalized Home Exercise Program in Patients With Bone Tumor Undergoing Lower Extremity Salvage Surgery
|
||
Recruiting |
NCT06180525 -
Radiological Evaluation of 3D Printed Porous Collars in Hip and Knee Resection Prostheses: Pilot Study.
|