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Completed

NCT Number: NCT00318240

Prostate Cancer Treatment Following Radiation Failure With High Intensity Focused Ultrasound (HIFU)

This is a feasibility study to determine safety and the ability of HIFU (High Intensity Focused Ultrasound)to selectively destroy prostate cancer tissue in men who demonstrate local recurrence of prostate cancer following radiation treatment.

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Key information

About this study

This is a feasibility study to determine the safety and the ability of HIFU (High Intensity Focused Ultrasound)to selectively destroy prostate cancer tissue in men who demonstrate local recurrence of prostate cancer following radiation treatment. All participants will receive treatment with HIFU and be monitored closely for recurrence of disease (if any),quality of life and adverse events.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • · Male patients with an initial presentation of organ confined recurrent prostate cancer (clinical Stages T1 and T2 only) who have been treated with external beam radiation therapy or brachytherapy and subsequently has biopsy-proven local recurrence.
  • Age > 40 years through <80 years.
  • Anesthesia Surgical Assignment (ASA) categories I, II or III only.
  • Negative radionuclide bone scan within 3 months prior to HIFU treatment to rule out the possibility of metastases.
  • PSA levels >0.5ng/ml and <10ng/ml.
  • Pre-radiation Gleason score < 8
  • Clearly imageable prostate on TRUS
  • Written informed consent.

Exclusion criteria

  • · T3 or T4 prostate cancer.
  • Age <40 years. or >80 years.
  • ASA of IV and higher.
  • Gleason score>8.
  • PSA <0.5ng/ml or >10ng/ml.
  • Prostate size > 40 grams as determined by transrectal ultrasound
  • Large calcification in the area to be treated (>5mm).
  • Bleeding disorder as determined by abnormal prothrombin time (INR)and partial thromboplastin time (PTT).
  • Patient on Coumadin or any other anticoagulant, unless their anticoagulation can 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 prostatic tissue adequately on transrectal ultrasound imaging.
  • Currently on hormonal therapy for prostate cancer (patients can be enrolled if they come off hormone therapy for 3 months).
  • History of treatment for prostate cancer, other than brachytherapy or external beam radiation.
  • 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.

Treatment and study plan

High Intensity Focused Ultrasound

Device

Treatment of Radiation failure in Prostate Cancer

Other names: HIFU

Primary outcomes

  1. To determine the efficacy of HIFU in men with local recurrent prostate cancer following radiation therapy.

    Time frame: ongoing

Secondary outcomes

  1. Destruction of prostate cancer tissue.

    Time frame: ongoing

  2. Safety of repeating procedure in patients who do not respond adequately.

    Time frame: ongoing

Sponsors and collaborators

Lead sponsor

London Health Sciences Centre Research Institute OR Lawson Research Institute of St. Joseph's

Other

Registry information

Official study title

Feasibility Study for Locally Recurrent Prostate Cancer Treatment Following Radiation Failure With High Intensity Focused Ultrasound (HIFU)

Important dates

Study start
2006
Primary completion
2009
Study completion
2009
First posted
Apr 26, 2006
Registry last updated
Aug 28, 2017

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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