Prostate Cancer Clinical Trial

Trial of Modifications to Radical Prostatectomy

Summary

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."

View Eligibility Criteria

Eligibility Criteria

Inclusion Criteria:

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

Exclusion Criteria:

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 or a node with abnormal morphology such as roundness or irregularity or loss of fatty hilum
Any prior pelvic radiation therapy used to treat prostate cancer

Hemostatic agent vs. no hemostatic agent

No additional exclusion criteria

Study is for people with:

Prostate Cancer

Phase:

Phase 3

Estimated Enrollment:

2600

Study ID:

NCT01407263

Recruitment Status:

Recruiting

Sponsor:

Memorial Sloan Kettering Cancer Center

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There are 3 Locations for this study

See Locations Near You

Memorial Sloan Kettering Cancer Center at Basking Ridge
Basking Ridge New Jersey, 07920, United States More Info
Andrew Vickers, PhD
Contact
646-888-8233
Memorial Sloan Kettering Westchester
Harrison New York, 10604, United States More Info
Andrew Vickers, PhD
Contact
646-888-8233
Memorial Sloan Kettering Cancer Center
New York New York, 10065, United States More Info
Andrew Vickers, PhD
Contact
646-888-8233
Peter Scardino, MD
Contact
646-422-4329
Andrew Vickers, PhD
Principal Investigator

How clear is this clinincal trial information?

Study is for people with:

Prostate Cancer

Phase:

Phase 3

Estimated Enrollment:

2600

Study ID:

NCT01407263

Recruitment Status:

Recruiting

Sponsor:


Memorial Sloan Kettering Cancer Center

How clear is this clinincal trial information?

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