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NCT01407263Active, not recruitingPhase 3

Trial of Modifications to Radical Prostatectomy

A Randomized Trial of Modifications to Radical Prostatectomy

Source: ClinicalTrials.gov · Last updated 17 Aug 2026

Brief summary (registry, in English)

This trial will evaluate whether the following aspect of surgical technique influence outcome: Lymph node dissection. In some patients, scans taken before surgery show that a lymph node has cancer. Surgeons make sure to remove those affect lymph nodes and all other lymph nodes in the area. However, it is not known whether removing lymph nodes helps prostate cancer patients whose scans do not show positive nodes. In this study, patients with clear scans will either receive a lymph node dissection or not."

Status (registry)
Active, not recruiting
Phase (registry)
Phase 3
Study type
Interventional
Enrollment
3204 (actual)
First submitted
29 Jul 2011
Start date
1 Jul 2011
Primary completion date
31 Jul 2027
Lead sponsor
Memorial Sloan Kettering Cancer Center
NCT number
NCT01407263

What you commit to

  • Study type: Interventional · Phase 3
  • Participants enrolled: 3204
  • From 1 Jul 2011 to the primary completion date, 31 Jul 2027
  • 5 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Any prior pelvic radiation therapy used to treat prostate cancer
    • Hemostatic agent vs. no hemostatic agent

Other

  • Lymphadenectomy vs no lymphadenectomy
  • Presence of positive/suspicious pelvic nodes on MRI, CT or PSMA scan (positive/suspicious defined as a pelvic node \>15mm in short axis on CT or MRI, a PSMA avid node, or a node with abnormal morphology such as roundness or irregularity or loss of fatty hilum)
  • No additional exclusion criteria

Who the study is looking for

  • Patients do not have to be eligible for both modifications to be included in the study.
    • Lymphadenectomy vs no lymphadenectomy:
  • Patients 21 years or older scheduled for radical prostatectomy for treatment of prostate cancer with one of the consenting surgeons at MSKCC
    • Hemostatic agent vs. no hemostatic agent
  • Patients 21 years or older scheduled for minimally invasive radical prostatectomy for the treatment of prostate cancer with one of the consenting surgeons at MSKC

Age in the registry: 21 years to - · Sex: Male · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (5)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Memorial Sloan Kettering Cancer Center at Basking Ridge
Coordinator of this site? Confirm its status
Basking RidgeUnited StatesUnknown status
Memorial Sloan Kettering Westchester
Coordinator of this site? Confirm its status
HarrisonUnited StatesUnknown status
Memorial Sloan Kettering Bergen (Consent Only)
Coordinator of this site? Confirm its status
MontvaleUnited StatesUnknown status
Memorial Sloan-Kettering Cancer Center
Coordinator of this site? Confirm its status
New YorkUnited StatesUnknown status
Memorial Sloan Kettering Cancer Center @ Nassau (Consent only)
Coordinator of this site? Confirm its status
UniondaleUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.