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Completed Phase 3 Interventional Results available

Cisplatin/Etoposide/Radiotherapy +/- Consolidation Docetaxel in Advanced Stage III Non-Small Cell Lung Cancer

ClinicalTrials.gov ID: NCT00216125

Public ClinicalTrials.gov record NCT00216125. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 5, 2026, 5:41 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase III Trial of Cisplatin/Etoposide/Radiotherapy With or Without Consolidation Docetaxel in Patients With Inoperable Locally Advanced Stage III Non-Small Cell Lung Cancer (NSCLC): Hoosier Oncology Group LUN01-24

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

In a previous phase II study, patients with pathological stage IIIb (without pleural effusion) NSCLC were treated with concurrent cisplatin and etoposide plus thoracic radiotherapy followed by 3 cycles of consolidation therapy with docetaxel. Docetaxel was selected based upon a survival benefit in patients with recurrent NSCLC. This trial will evaluate the role of consolidation therapy with docetaxel in patients with unresectable stage III disease. The purpose of the trial is to evaluate survival and toxicities of the regimens employed.

Study identification

NCT ID
NCT00216125
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Nasser Hanna, M.D.
Other
Enrollment
243 participants

Conditions and interventions

Interventions

Drug · Radiation

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jan 31, 2002
Primary completion
May 31, 2006
Completion
Feb 29, 2008
Last update posted
Mar 15, 2016

2002 – 2008

United States locations

U.S. sites
15
U.S. states
5
U.S. cities
13
Facility City State ZIP Site status
Medical & Surgical Specialists, LLC Galesburg Illinois 61401
Elkhart Clinic Elkhart Indiana 46515
Oncology Hematology Associates of SW Indiana Evansville Indiana 47714
Fort Wayne Oncology & Hematology, Inc Fort Wayne Indiana 46815
Center for Cancer Care at Goshen Health System Goshen Indiana 46527
Indiana University Cancer Center Indianapolis Indiana 46202
Quality Cancer Center (MCGOP) Indianapolis Indiana 46202
Community Regional Cancer Center Indianapolis Indiana 46256
Medical Consultants, P.C. Muncie Indiana 47303
Center for Cancer Care, Inc., P.C. New Albany Indiana 47150
Northern Indiana Cancer Research Consortium South Bend Indiana 46601
AP&S Clinic Terre Haute Indiana 47804
Siteman Cancer Center St Louis Missouri 63110
Methodist Cancer Center Omaha Nebraska 68114
US Oncology Houston Texas 77060

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00216125, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Mar 15, 2016 · Synced Sep 5, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00216125 live on ClinicalTrials.gov.

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