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NCT05610852Toboroz

Single-Port Transvesical Partial Prostatectomy Versus High Intensity Focused Ultrasound

Prospective Single-Center Randomized Study Of Single-Port Transvesical Partial Prostatectomy Versus High Intensity Focused Ultrasound (HIFU)

Forrás: ClinicalTrials.gov · Utoljára frissítve: 2026. aug. 6.

Következő lépések

Rövid összefoglaló (regiszter, angolul)

This study aims to compare the novel single-port robotic partial prostatectomy to High-intensity focused ultrasound (HIFU) in patients with low to intermediate risk localized prostate cancer. These interventions have become acceptable focal therapies prevalent with beneficial oncologic outcomes and therefore need to be examined further.

Állapot (regiszter)
Toboroz
Vizsgálattípus
Beavatkozással járó
Résztvevők száma
276 (tervezett)
Első benyújtás
2022. okt. 31.
Kezdés
2024. jan. 1.
Elsődleges befejezés
2026. dec. 1.
Fő szponzor
Case Comprehensive Cancer Center
Betegségek
Prosztatarák
NCT-szám
NCT05610852

Mit vállalsz

  • Vizsgálat típusa: Beavatkozással járó
  • Tervezett résztvevők: 276
  • 2024. jan. 1. és az elsődleges befejezés (2026. dec. 1.) között
  • 1 helyszín, 1 országban
  • Vizitek és vizsgálatok: kérdezd a vizsgálat csapatát, a regiszter nem sorolja fel őket

A(z) ClinicalTrials.gov regisztermezőiből összeállítva. A vizsgálat felépítését írja le.

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Korábbi kezelés

  • Patients with any prior extensive pelvic surgery, pelvic fractures, hemorrhoid, fissure surgery, cardiac pacemaker, or metal prosthesis
  • Prior treatment for prostate cancer such as radiotherapy, focal or hormonal therapy
  • Poor surgical risk (defined as American Society of Anesthesiology score > 3).

Más betegség

  • Uncorrected coagulopathy or history of Latex allergy
  • Active soft tissue or urinary infection, indwelling Foley catheter or severe irritative or obstructive symptoms
  • Any condition or history of illness or surgery that, in the opinion of the investigator, might confound the results of the study or pose additional risk to the patient (e.g. significant cardiovascular conditions that significantly affect the life expectancy, chronic opiate use, pain syndrome, or drug abuse.)
  • Subjects with uncontrolled intercurrent illness including, but not limited to ongoing or active infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia, or psychiatric illness/social situations that would limit compliance with study requirements.

Egyéb

  • Prostate size larger than 80 grams.
  • Subjects with prostatic Calcification (>0.5 cc) close to the area to be treated.
  • Subjects with extraprostatic extension or cribriform pattern on biopsy.
  • Subjectes with sexual dysfunction defined as SHIM score < 17

Kiket keres a vizsgálat

  • Subjects must have histologically or cytologically: Biopsy-confirmed prostate cancer, stage T1a, T2a, T2b, or T2c prostate cancer using MRI staging, with a region of interest (ROI) PIRADs grade 3 or greater, Serum PSA 10 ng/ml or less, Region of interest on MRI of grade 3 or greater
  • The MRI performed must include at least:
  • A T2-weighted sequence in sections ≤ 4 mm, centered on the prostate and seminal vesicles, at least in the axial plane. Alternatively, a 3D T2-weighted sequence can be realized,
  • A diffusion sequence of ≤ 4 mm slice in the axial plane. An ADC card will be provided and calculated from at least two values of b, the maximum value of b being ≥ 600 s / mm2,
  • A dynamic sequence after gadolinium injection. It will be a sequence of echo T1-weighted gradient of slice ≤ 4 mm, centered on the prostate and seminal vesicles in the axial plane, with or without fat saturation. A first series will be performed without contrast injection, and will be repeated iteratively for the arrival of a bolus of gadolinium chelates. The time resolution (that is to say, the acquisition time of one dynamic series will be ≤ 20 seconds). The number of chained dynamic series is calculated so that the total length of the dynamic acquisition be at least 3 minutes
  • A total dose of 0.1 mmol / kg of gadolinium chelate will be injected at a rate of 3-4 mL / s by using an automatic injector, in a vein of the hand of the forearm or elbow.
  • If necessary, subtracted images are calculated
  • Clinically significant prostate cancer defined as Gleason score 3+4 or less in any core
  • Biopsies for preoperative diagnosis of prostate cancer will have included: At least 12 randomized samples (2 samples per sextant), At least two targeted sampling on each target score MRI ESUR ≥ 3/5
  • Life expectancy greater than 10 years.
  • Age >18 years.
  • Subjects must have the ability to understand and the willingness to sign a written informed consent document.

Életkor a regiszterben: 19 év – - · Nem: csak férfiak · Egészséges önkénteseket nem fogad

A teljes feltétellista: ClinicalTrials.gov

Helyszínek (1)

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HelyszínVárosOrszágHelyszín állapota
Glickman Urological & Kidney Institute, Cleveland Clinic Foundation, Case Comprehensive Cancer CenterClevelandEgyesült ÁllamokToboroz

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