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Treatment of Localized Prostate Cancer With High Intensity Focused Ultrasound Using the Sonablate® 500 System in Canada
This study is not yet open for participant recruitment.
Study NCT00573586   Information provided by USHIFU, LLC
First Received: December 12, 2007   Last Updated: December 13, 2007   History of Changes

December 12, 2007
December 13, 2007
March 2008
 
PSA level [ Time Frame: PSA level at 30 and 90 days post treatment ] [ Designated as safety issue: No ]
Same as current
Complete list of historical versions of study NCT00573586 on ClinicalTrials.gov Archive Site
 
 
 
Treatment of Localized Prostate Cancer With High Intensity Focused Ultrasound Using the Sonablate® 500 System in Canada
Investigational Study For the Treatment of Localized (T1c/T2a) Prostate Cancer With High Intensity Focused Ultrasound (HIFU) Using the Sonablate® 500 (SB-500) System in Canada

This is an investigational study on the use of high intensity focused ultrasound (HIFU) in the management of localized prostate cancer (T1c/T2a) as a primary non-comparative study.

High intensity focused ultrasound (HIFU) is a non-invasive acoustic ablation technique that uses intersecting, precision focused ultrasound waves to raise the temperature of the target to) 80-90 degrees C in 2-3 seconds, destroying the targeted tissues (prostate cancer). The tissue targeting is highly precise, minimizing collateral damage.

The overall hypothesis is that HIFU with Sonablate can safely, effectively and selectively ablate prostate cancer tissue, resulting in complete tissue necrosis, in patients diagnosed with localized T1c/T2a prostate cancer, with minimal morbidity.

The specific hypothesis is that the Sonablate has the ability to:

  • Completely destroy prostate cancer tissue, without causing damage to the intervening tissue, with a drop in PSA levels to <0.5ng/ml.
  • Result in negative biopsies for evidence of viable malignant cells after the treatment (12 months if Nadir is not reached or PSA rises from Nadir)
  • Safely treat localized prostate cancer patients, with minimal and acceptable adverse effects
 
Phase IV
Interventional
Treatment, Non-Randomized, Open Label, Uncontrolled, Single Group Assignment, Safety/Efficacy Study
Prostate Cancer
Device: Sonablate 500 (SB-500)
 
 

*   Includes publications given by the data provider as well as publications identified by National Clinical Trials Identifier (NCT ID) in Medline.
 
Not yet recruiting
20
March 2009
 

Inclusion Criteria:

  • Male patients with an initial presentation of organ confined prostate cancer;(clinical stages T1c and T2a only)
  • Age 40 yrs. and older up to and including age 80 yrs.
  • Anesthesia Surgical Assignment (ASA) categories I, II or III only
  • PSA levels equal tyo or less than 10ng/ml
  • Pre-HIFU Gleason score equal to or less than 7
  • Clearly imageable prostate on TRUS
  • Prostate total volume less than 40cc with an AP height less than or equal to 4.2cm. (If volume is greater than 40cc or height greater than 4.2 cm, one 3 monthly shot of an LHRH analogue may be provided, followed by re-imaging of the prostate to document total volume below 40cc.)

Exclusion Criteria:

  • Large calcification in the area to be treated (>5mm)
  • Bleeding disorder as determined by abnormal prothrombin time (INR) and partial thromboplastin time (PTT)
  • Pt. on Coumadin or any other anticoagulent, unless their anticoagulation an be temporarily reversed or stopped
  • Urinary tract infection unless treated satisfactorily by antibiotics and documented by a sterile urine culture
  • Interest in future fertility
  • History of allergy to latex
  • Inability to visualize the prostate tissue adequately on transrectal ultrasound imaging
  • History of treatment for prostate cancer (except for one LHRH analogue "shrinkage shot")
  • History of TURP, thermotherapy or urethral stent
  • History of any major rectal surgery
  • History of inflammatory bowel disease
  • History of urinary bladder neck contracture
  • History of any other malignancy other than skin cancer. Patients that have had a previous malignancy and no recurrence of that malignancy within the past 5 years will be allowed; (superficial bladder cancer is OK of clear for 2 years)
  • Inability to be placed in lithotomy position Prior long term hormonal therapy for prostate cancer (including bilateral orchiectomy).
Male
40 Years to 80 Years
No
Contact: George Vrabec, MD gvrabec@hotmail.com
Canada
 
NCT00573586
George Vrabec, MD, Principle Investigator
USHIFU-CABC-PC002
USHIFU, LLC
 
Principal Investigator: George Vrabec, MD Abbotsford Regional Hospital Cancer Center
USHIFU, LLC
December 2007

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP