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NCT02225925 · ClinicalTrials.gov registry record · NA

Intraoperative Dosimetry for Prostate Brachytherapy Using Fluoroscopy and Ultrasound

A NA study of Prostate Cancer and Adenocarcinoma of the Prostate, sponsored by Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins.

Completed
Registry status
NA
Development phase
45
Enrollment target
1
Study location

NCT02225925 is a NA study of Prostate Cancer and Adenocarcinoma of the Prostate that has completed, run by Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins. The registered enrollment target is 45 participants, below the 608-participant average among 735 other Prostate Cancer trials with a reported enrollment target (93% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT02225925, a NA study of Prostate Cancer and Adenocarcinoma of the Prostate, has completed, sponsored by Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins.

COMPLETED
Registry status
NA
Development phase
45 participants
Enrollment target
1
Study location

Study Summary

The purpose of this study is to assess the performance of a system of intraoperative dynamic dosimetry during prostate seed implantation (brachytherapy) including its new elements, to evaluate and refine technical methods of using the system, as well as confirm its performance and accuracy.

Interventions

  • RADIATION Brachytherapy

Study Locations (1)

Maryland

  • The SKCCC at Johns Hopkins - Baltimore

Trial Details

FieldValue
Enrollment Target 45 participants
Start Date 2014-10-01
Est. Completion 2023-02-28
Phase NA

What the Registry Record Tells You About NCT02225925

The ClinicalTrials.gov registry entry for NCT02225925 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 45 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 608-participant average among 735 other Prostate Cancer trials with a reported enrollment target (93% lower). The listed sponsor is Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins, which has 523 total studies on file at ClinicalTrials.gov.

The record links to 2 conditions, with Prostate Cancer appearing as the primary indexed condition, and to 1 intervention - of which Brachytherapy is the first listed.

NCT02225925 reports 1 study location spanning 1 distinct geographic area - top geographies include Maryland.

Frequently Asked Questions

What is clinical trial NCT02225925 about?

NCT02225925 is a clinical study titled "Intraoperative Dosimetry for Prostate Brachytherapy Using Fluoroscopy and Ultrasound". The purpose of this study is to assess the performance of a system of intraoperative dynamic dosimetry during prostate seed implantation (brachytherapy) including its new elements, to evaluate and refine technical methods of using the system, as well as confirm its performance and accuracy.

What is the current status of trial NCT02225925?

This trial is currently completed. It is a NA study. The enrollment target is 45 participants. The study started on 2014-10-01. Estimated completion is 2023-02-28.

What conditions does trial NCT02225925 study?

This clinical trial studies the following conditions: Prostate Cancer, Adenocarcinoma of the Prostate.

What interventions are being tested in trial NCT02225925?

The interventions under investigation include: Brachytherapy (RADIATION).

Who is sponsoring clinical trial NCT02225925?

This trial is sponsored by Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins, which has 523 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT02225925 being conducted?

This trial has 1 study location across Maryland. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

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