Clinical trial · Observational
Pilot Study to Develop 3 Tesla MRI for Evaluation of Renal Tumors
NCT00507884CI-TRIAL-00049216unknownClinicalTrials.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 goal of this clinical research study is to find out if "3 Tesla" MRI is as good as CT scan in the evaluation of kidney tumor(s). Objectives: To provide preliminary data to enable subsequent development of an MRI protocol at 3 Tesla for evaluation of renal tumors and their vascular supply, which can be adopted in patients who are unable to undergo CT evaluation.
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Kidney Neoplasms | Kidney Neoplasm | ONTOLOGY_EXACT | 0.90 |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| 3 Tesla MRI Scan | Procedure | — | UNRESOLVED |
Design
Arms and outcomes
Arms (1)
- label
- 3 Tesla MRI
- description
- Patients with renal tumors scheduled to have a CT scan of the kidneys and abdomen.
- interventionNames
- Procedure: 3 Tesla MRI Scan
Primary outcomes (1)
- measure
- Comparison of CT and MRI scans of patients with renal cell carcinoma in evaluating each of nine imaging variables.
- timeFrame
- 4 Years
Eligibility
Eligibility (as posted)
- Sex
- All
Show eligibility criteria text
Inclusion Criteria: 1. Patients who have undergone or are due to undergo a CT Renal Protocol study, in the course of pre-operative evaluation for renal tumor surgery. 2. Written informed consent will be obtained. Exclusion Criteria: 1. Patients with an allergy to both gadopentetate dimeglumine and gadodiamide MRI contrast agents. 2. Patients with certain metallic implants, e.g., cardiac pacemakers, cardiac defibrillators, aneurysm clips, neurostimulators, and certain metallic foreign bodies. Implanted medical devices must be MRI compatible at 3.0 Tesla field strengths. 3. Patients with claustrophobia, or requiring sedation for the MRI scan.
References
Publications (0)
Data not yet available
No reference posted for this study.