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Clinical Trials/NCT02076503
NCT02076503
Completed
Not Applicable

Pre-operative PET-MR of High Risk Prostate Cancer Patients for Assessment of Cancer Aggressiveness and Lymph Node Status

St. Olavs Hospital1 site in 1 country28 target enrollmentApril 2014

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Prostatic Neoplasms
Sponsor
St. Olavs Hospital
Enrollment
28
Locations
1
Primary Endpoint
Positive and negative predictive value of 18FACBC PET/MR for detection of lymph node metastases
Status
Completed
Last Updated
8 years ago

Overview

Brief Summary

Prostate cancer is the most frequent cancer in Norwegian men. For optimal treatment, accurate staging of the disease at the time point of diagnosis is important. The objective of this study is to evaluate the diagnostic potential of a combined PET/MR examination for risk assessment and detection of lymph node metastases. The overall aim of the project is to improve the investigators ability to provide individually tailored treatment to prostate cancer patients.

The study will include 32 men with high-risk prostate cancer, who are eligible for radical prostatectomy. Informed consent is a requirement for inclusion in the study.

Registry
clinicaltrials.gov
Start Date
April 2014
End Date
May 2015
Last Updated
8 years ago
Study Type
Interventional
Study Design
Single Group
Sex
Male

Investigators

Sponsor
St. Olavs Hospital
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • High-risk prostate cancer according to EAU guidelines (Gleason score ≥8 and/or PSA ≥20 ng/ml and/or ≥ cT3a cancer)
  • Eligibility for the surgical procedure (radical prostatectomy and bilateral pelvic lymph node resection)

Exclusion Criteria

  • Previous treatment (for example TURP or hormone therapy)
  • Contraindication for the PET/MR examination (including, but not limited to: pacemaker, aneurysm clips, reduced renal function, metal implants, claustrophobia)

Outcomes

Primary Outcomes

Positive and negative predictive value of 18FACBC PET/MR for detection of lymph node metastases

Time Frame: 7 days

Findings on 18FACBC PET/MR images will be compared to histopathology, which is considered the gold standard for evaluation of pelvic lymph node metastases

Study Sites (1)

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