跳至主要内容
临床试验/ACTRN12612000523808
ACTRN12612000523808招募中未知

Patients with prostate cancer scheduled for a prostatectomy to have an Irreversible Electroporation procedure two to four weeks prior to the prostatectomy for the researchers to determine the effectiveness of irreversible electroporation on a small region in the prostate.

Flack Trustees0 个研究点目标入组 6 人开始时间: 2012年5月16日最近更新:
适应症

试验速览

阶段
未知
状态
招募中
发起方
入组人数
6

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional
分配方式
Non-randomised trial
主要目的
Treatment
盲法
Open (masking not used)

入排标准

年龄范围
40 Years 至 75 Years(—)
性别
Male

入选标准

  • 1. 40 - 75 years 2. Histologically confirmed organ-confined prostate cancer (clinical stage T1-T2a) 3. Gleason score 7 (3+4 only) or less 4. PSA less than or equal to 10 ng/ml 5. No significant intravesical median lobe on ultrasound 6. Able to visualize prostate gland adequately on transrectal US imaging 7. No prostate calcification greater than 5 mm 8. Ability of subject to stop anticoagulant and anti-platelet therapy for 7 days prior and 7 days post procedure

排除标准

  • 1. <40, >75 years of age 2. High to medium risk subject with any one of the following: a) PSA greater than 10ng/ml, b) Gleason 7 (4+3 only) or greater, c) Positive bone scan 3. Other Conditions/Status a) Bleeding disorder as determined by prothrombin time (PT) > 14.5 seconds, partial thromboplastin time (PTT) > 34 seconds, and platelet count < 140/uL b) Active urinary tract infection (UTI”) c) History of bladder neck contracture d) Anaesthesia Surgical Assignment, category IV or greater e) Interest in future fertility f) History of inflammatory bowel disease g) Concurrent major debilitating illness h) Prior or concurrent malignancy 4. Prior or current therapies a) Biologic therapy for prostate cancer b) Chemotherapy for prostate cancer c) Hormonal therapy for prostate cancer within 3 months of procedure d) Radiotherapy for prostate cancer e) Transurethral prostatectomy (TURP), urethral stent f) Prior major rectal surgery (except haemorrhoids) g) Inability or unwillingness to tolerate temporary cessation of concurrent anticoagulation therapy or anti-platelet drugs for a period of 7days prior to procedure and up to 7 days after procedure

研究者

发起方
Flack Trustees

相似试验

招募中
不适用
Prostate cancer background, QOL, patient&#39;s satisfaction and treatment survey by Japan Prostate Cancer Study GroupProstate cancer
JPRN-UMIN000004666J-CaP study group10,000
已完成
不适用
Patient involvement in prostate cancer treatment decisionsCancerProstate cancer
ISRCTN97145188Dutch Cancer Society (The Netherlands)300
尚未招募
2 期
A continence promotion intervention involving a pelvic floor muscle rehabilitation exercise program to reduce lower urinary tract, lower bowel symptoms and erectile dysfunction in men receiving radiation therapy with or without androgen deprivation therapy (ADT): A Pilot StudyProstate Cancer TreatmentLower Urinary Tract sequelae to radiation therapy with or without androgen deprivation therapyLower Bowel Dysfunction as sequelae to radiation therapy with or without androgen deprivation therapyErectile Dysfunction as sequelae to radiation therapy with or without androgen deprivation therapyCancer - ProstatePhysical Medicine / Rehabilitation - PhysiotherapyRenal and Urogenital - Other renal and urogenital disorders
ACTRN12612000527864niversity of Newcastle40
已完成
1 期
Radionuclide therapy using Lutetium-177 prostate specific membrane antigen (PSMA): a pilot study in men with castrate-resistant prostate cancer (LuPSMA trial)Cancer - ProstateProstate Cancer
ACTRN12615000912583Peter MacCallum Cancer Centre30
招募中
不适用
PROCOG: Investigating Cognitive Problems in Men with Prostate CancerCognitive problemsCancer - ProstateMental Health - Studies of normal psychology, cognitive function and behaviourMental Health - AnxietyMental Health - DepressionMental Health - Other mental health disordersProstate Cancer
ACTRN12621001608853Macquarie University150