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NCT00669162 · ClinicalTrials.gov registry record · Phase 1

Postoperative Radiation Therapy, Hormonal Therapy and Concurrent Docetaxel for High Risk Pathologic Prostate Cancer

A Phase 1 study of Prostate Cancer, sponsored by University of Kansas Medical Center.

Completed
Registry status
Phase 1
Development phase
27
Enrollment target
1
Study location

NCT00669162 is a Phase 1 study of Prostate Cancer that has completed, run by University of Kansas Medical Center. The registered enrollment target is 27 participants, below the 608-participant average among 735 other Prostate Cancer trials with a reported enrollment target (96% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT00669162, a Phase 1 study of Prostate Cancer, has completed, sponsored by University of Kansas Medical Center.

COMPLETED
Registry status
Phase 1
Development phase
27 participants
Enrollment target
1
Study location

Study Summary

Following a radical prostatectomy and lymph node sampling, eligible patients will undergo post-operative radiation therapy, concurrent weekly docetaxel chemotherapy , and hormonal therapy (Casodex daily and Zoladex every 3 months for 2 times or Lupron 22.5 mg im every 3 months for 2 times).

Conditions Studied

Interventions

  • DRUG Docetaxel
  • RADIATION Radiation Therapy
  • DRUG Casodex and Zoladex (or Lupron)

Study Locations (1)

Kansas

  • University of Kansas Medical Center - Kansas City

Trial Details

FieldValue
Enrollment Target 27 participants
Start Date 2012-08
Est. Completion 2017-04
Phase Phase 1

Sponsor

University of Kansas Medical Center

408 total trials

What the Registry Record Tells You About NCT00669162

The ClinicalTrials.gov registry entry for NCT00669162 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 27 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 (96% lower). The listed sponsor is University of Kansas Medical Center, which has 408 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Prostate Cancer appearing as the primary indexed condition, and to 3 interventions - of which Docetaxel is the first listed.

NCT00669162 reports 1 study location spanning 1 distinct geographic area - top geographies include Kansas.

Frequently Asked Questions

What is clinical trial NCT00669162 about?

NCT00669162 is a clinical study titled "Postoperative Radiation Therapy, Hormonal Therapy and Concurrent Docetaxel for High Risk Pathologic Prostate Cancer". Following a radical prostatectomy and lymph node sampling, eligible patients will undergo post-operative radiation therapy, concurrent weekly docetaxel chemotherapy , and hormonal therapy (Casodex daily and Zoladex every 3 months for 2 times or Lupron 22.5 mg im every 3 months for 2 times).

What is the current status of trial NCT00669162?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 27 participants. The study started on 2012-08. Estimated completion is 2017-04.

What conditions does trial NCT00669162 study?

This clinical trial studies the following conditions: Prostate Cancer.

What interventions are being tested in trial NCT00669162?

The interventions under investigation include: Docetaxel (DRUG), Radiation Therapy (RADIATION), Casodex and Zoladex (or Lupron) (DRUG).

Who is sponsoring clinical trial NCT00669162?

This trial is sponsored by University of Kansas Medical Center, which has 408 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT00669162 being conducted?

This trial has 1 study location across Kansas. 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

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.