Detection of Lymphnodes Using ICG During RARP

NCT02163083 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 120

Last updated 2019-01-18

No results posted yet for this study

Summary

The purpose of this study is to investigate, whether the detection of lymph nodes by means of intraoperative fluorescence lymphography as part of lymphadenectomy in robot-assisted radical prostatectomy is higher than without the use of indocyanine green (ICG).

Conditions

Interventions

PROCEDURE

ICG

Improvement of detection of positive lymphnodes

Sponsors & Collaborators

  • St. Antonius Hospital Gronau

    lead OTHER

Principal Investigators

  • Jörn H. Witt, MD · St. Antonius Hospital Gronau

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
75 Years
Sex
MALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2014-08-31
Primary Completion
2015-04-30
Completion
2017-04-30

Countries

  • Germany

Study Locations

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02163083 on ClinicalTrials.gov