Clinical trial · Interventional
Using Fiducial Markers to Aid in Prostate Cancer Radiation Treatment
Trans-Rectal Placement of Prostatic Fiducial Markers Under MR-Guidance in Patients Receiving External Beam Radiotherapy for Prostate Cancer: A Pilot Study
- 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)
To effectively treat prostate cancer, doctors need an accurate view (via X-rays) of the prostate gland during radiation therapy. To help improve this view, doctors may insert gold markers called fiducials into the prostate by placing hollow gold needles through the rectum and moving a fiducial through each needle. The purpose of the study is to determine whether an MRI scan can help doctors improve their placement of these needles. Fifteen men will participate in this study. Patients will take the antibiotic levofloxacin for two days prior to the placement of the fiducials, then will have a small enema and another dose of the antibiotic on the morning of the procedure. After being anesthetized, patients will have an antenna-like tube placed into the rectum and have MRI images taken of the area. The doctor will then use these scans to place four fiducials into the prostate. The procedure will require approximately 45 minutes. Patients will be allowed to go home the same day of the procedure, which will be followed by a seven-week course of standard radiation therapy. Prior to their participation in this study, patients will undergo the following evaluations: a physical exam, blood work, urine tests, and, if appropriate, an MRI or bone scan.
Conditions
Conditions (2)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Cancer | Malignant Neoplasm | ALIAS | 0.90 |
| Prostate Cancer | Malignant Prostate Neoplasm | CURATED_EXACT | 0.92 |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Fiducial marker placement | Procedure | — | UNRESOLVED |
Design
Arms and outcomes
Arms (1)
- type
- EXPERIMENTAL
- label
- 1
- description
- Placement of fidicual markers under MRI guidance for localization of radiaiton treatment
- interventionNames
- Procedure: Fiducial marker placement
Primary outcomes (2)
- measure
- To test the hypothesis that MRI guidance allows for accurate fiducial marker placement within the prostate
- timeFrame
- 1, 3, 6, 12, 18, 24, 36, 48, and 60 months
- measure
- To determine the toxicity of MR-Guided fiducial marker placement
- timeFrame
- 1, 3, 6, 12, 18, 24, 36, 48, and 60 months
Secondary outcomes (5)
- measure
Eligibility
Eligibility (as posted)
- Sex
- Male
- Minimum age
- 18 Years
- Maximum age
- 90 Years
Show eligibility criteria text
* INCLUSION CRITERIA: * Pathologically confirmed adenocarcinoma of the prostate gland. * Age greater than or equal to 18 years. * ECOG performance status of 0 or 1. * Informed consent: All patients must sign a document of informed consent indicating their understanding of the investigational nature and risks of the study before any protocol related studies are performed (this does not include routine laboratory tests or imaging studies required to establish eligibility). EXCLUSION CRITERIA: Patients with contraindication to transrectal needle placement: * Bleeding disorder; * PT/PTT greater than 1.5.times the upper limit of normal; * Platelets less than 50K; * Artificial heart valve. Patients with contraindications to MRI: * Patients weighing greater than 136 kg (weight limit for scanner table); * Patients with pacemakers, cerebral aneurysm clips, shrapnel injury, or implanted electronic devices. * Patients with chronic inflammatory bowel disease. * Patients with distant metastatic disease. * Patients with a prior history of pelvic or prostate radiotherapy. * Cognitively impaired patients who cannot give informed consent. * Other medical conditions deemed by the PI or associates to make the patient ineligible for protocol investigations, procedures, and high-dose external beam radiotherapy.
References
Publications (3)
- BACKGROUNDYu KK, Hricak H. Imaging prostate cancer. Radiol Clin North Am. 2000 Jan;38(1):59-85, viii. doi: 10.1016/s0033-8389(05)70150-0. PMID 10664667
- BACKGROUNDKnopp MV, Weiss E, Sinn HP, Mattern J, Junkermann H, Radeleff J, Magener A, Brix G, Delorme S, Zuna I, van Kaick G. Pathophysiologic basis of contrast enhancement in breast tumors. J Magn Reson Imaging. 1999 Sep;10(3):260-6. doi: 10.1002/(sici)1522-2586(199909)10:33.0.co;2-7. PMID 10508285
- BACKGROUNDKurhanewicz J, Vigneron DB, Hricak H, Narayan P, Carroll P, Nelson SJ. Three-dimensional H-1 MR spectroscopic imaging of the in situ human prostate with high (0.24-0.7-cm3) spatial resolution. Radiology. 1996 Mar;198(3):795-805. doi: 10.1148/radiology.198.3.8628874. PMID 8628874