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NCT00232206 · ClinicalTrials.gov registry record · Phase 2

Trial of Neoadjuvant Docetaxel and Cisplatin for Resectable Non-Small Cell Lung Cancer

A Phase 2 study, sponsored by Providence Health & Services.

Terminated
Registry status
Phase 2
Development phase
40
Enrollment target

NCT00232206 is a Phase 2 study that was terminated before completion, run by Providence Health & Services. The registered enrollment target is 40 participants.

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The verdict

NCT00232206, a Phase 2 study, was terminated before completion, sponsored by Providence Health & Services.

TERMINATED
Registry status
Phase 2
Development phase
40 participants
Enrollment target

Study Summary

The primary objective of this study is to assess the response rate of treatment with two cycles of cisplatin and docetaxel chemotherapy prior to surgery (neoadjuvant) for early stage non-small cell lung cancer (NSCLC). Secondary objectives of this study include assessment of radiographic response rate by computed tomography (CT) scanning, overall survival, time to progression, rate of complete surgical removal, and adverse reactions. In addition, this study will test whether positron emission tomography (PET) imaging can predict a tumor response. Patients who have a response to chemotherapy may receive 2 additional cycles after recovering from surgery.

Interventions

  • DRUG Neoadjuvant Therapy with Cisplatin Plus Docetaxel

Trial Details

FieldValue
Enrollment Target 40 participants
Start Date 2005-05
Est. Completion 2007-11
Phase Phase 2

Sponsor

Providence Health & Services

69 total trials

What the Registry Record Tells You About NCT00232206

The ClinicalTrials.gov registry entry for NCT00232206 describes a study currently listed as terminated, categorized as Phase 2. The registered enrollment target is 40 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Providence Health & Services, which has 69 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 1 intervention - of which Neoadjuvant Therapy with Cisplatin Plus Docetaxel is the first listed.

NCT00232206 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT00232206 about?

NCT00232206 is a clinical study titled "Trial of Neoadjuvant Docetaxel and Cisplatin for Resectable Non-Small Cell Lung Cancer". The primary objective of this study is to assess the response rate of treatment with two cycles of cisplatin and docetaxel chemotherapy prior to surgery (neoadjuvant) for early stage non-small cell lung cancer (NSCLC). Secondary objectives of this study include assessment of radiographic response ra...

What is the current status of trial NCT00232206?

This trial is currently terminated. It is a Phase 2 study. The enrollment target is 40 participants. The study started on 2005-05. Estimated completion is 2007-11.

What interventions are being tested in trial NCT00232206?

The interventions under investigation include: Neoadjuvant Therapy with Cisplatin Plus Docetaxel (DRUG).

Who is sponsoring clinical trial NCT00232206?

This trial is sponsored by Providence Health & Services, which has 69 total clinical trials registered on ClinicalTrials.gov.

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

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.