Clinical trial · Observational
Cook iMRI Needles NSR Clinical Study
Cook® iMRI Needles Non-Significant Risk Clinical Study
NCT07783698CI-TRIAL-00124416completedClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
The purpose of this study is to evaluate the safety and performance of the Cook® iMRI Needle. This is an investigational needle that physicians can use to gain access to a particular part of the body, take a small sample of tissue, or inject fluid into a particular part of the body.
Conditions
Conditions (3)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Masses | — | UNRESOLVED | — |
| Tumors (Others) | Neoplasm | ALIAS | 0.85 |
| Viscera | — | UNRESOLVED | — |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Percutaneous non-vascular access to anatomic structures | Device | — | UNRESOLVED |
Design
Arms and outcomes
Arms (1)
- label
- Patient Cohort
- interventionNames
- Device: Percutaneous non-vascular access to anatomic structures
Primary outcomes (1)
- measure
- Rate of successful needle introduction
- timeFrame
- Duration of procedure (approximately 1 hour)
- description
- Successful percutaneous needle introduction into the target anatomy.
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
Show eligibility criteria text
Inclusion Criteria: Patient is suitable for inclusion in the study if the patient meets the following criteria: 1. A qualified physician directs the patient to have a procedure that requires a needle for percutaneous access, aspiration, and/or injection during therapeutic or diagnostic interventional MRI-guided procedures 2. Patients, or their legally authorized representatives, must also voluntarily consent to participate in the study Exclusion Criteria: 1. Inability or refusal to give informed consent by the patient or legally authorized representative 2. Age \< 18 years 3. Vulnerable population (specifically prisoners, lactating women and/or cognitively impaired patients) 4. Patients lacking a safe trajectory to the target tissue, as determined by the physician 5. Patients with uncorrectable coagulopathy 6. Allergy to the device or contrast media that cannot be adequately premedicated 7. Body habitus or medical condition that compromises or prevents necessary imaging procedures 8. Body weight exceeding limits of available MRI machines 9. Target lesion is unable to be reached by the longest needle (or in combination with a core biopsy device) 10. Implanted non-MR conditional device or other metallic device (e.g., certain pacemakers, aneurysm clips, cochlear implants, and/or mechanical heart valves) 11. Inability of the patient to cooperate with, or to be positioned for, the procedure
References
Publications (0)
Data not yet available
No reference posted for this study.