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COMPLETED NA

Early Detection of Second Lung Cancer in Patients With Stage I Non-small Cell Lung Cancer

NCT00002667 · View on ClinicalTrials.gov ↗

Study Summary

RATIONALE: Using new methods to examine sputum samples for the presence of cancer cells may detect lung cancer earlier. PURPOSE: Screening trial to study the effectiveness of new methods of examining sputum samples to detect second primary lung cancer in patients with resected stage I non-small cell lung cancer.

Conditions Studied

Interventions

  • OTHER cytology specimen collection procedure
  • PROCEDURE study of high risk factors
  • OTHER immunoenzyme technique

Study Locations (5)

Florida

  • H. Lee Moffitt Cancer Center and Research Institute — Tampa

Iowa

  • CCOP - Iowa Oncology Research Association — Des Moines

New Jersey

  • CCOP - Northern New Jersey — Hackensack

Ohio

  • Ireland Cancer Center — Cleveland

Pennsylvania

  • Allegheny University Hospitals- Hahnemann — Philadelphia

Trial Details

FieldValue
Enrollment Target 1,100 participants
Start Date 1995-10-10
Est. Completion 2004-10-01
Phase NA

Sponsor

Eastern Cooperative Oncology Group

30 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT00002667

The ClinicalTrials.gov registry entry for NCT00002667 describes a study currently listed as completed. It is categorized as NA, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 1,100 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Eastern Cooperative Oncology Group, which has 30 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Lung Cancer appearing as the primary indexed condition, and to 3 interventions — of which cytology specimen collection procedure is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT00002667 reports 5 study locations spanning 5 distinct geographic areas — top geographies include Florida, Iowa, New Jersey. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT00002667 about?

NCT00002667 is a clinical study titled "Early Detection of Second Lung Cancer in Patients With Stage I Non-small Cell Lung Cancer". RATIONALE: Using new methods to examine sputum samples for the presence of cancer cells may detect lung cancer earlier. PURPOSE: Screening trial to study the effectiveness of new methods of examining sputum samples to detect second primary lung cancer in patients with resected stage I non-small cel...

What is the current status of trial NCT00002667?

This trial is currently completed. It is a NA study. The enrollment target is 1,100 participants. The study started on 1995-10-10. Estimated completion is 2004-10-01.

What conditions does trial NCT00002667 study?

This clinical trial studies the following conditions: Lung Cancer. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT00002667?

The interventions under investigation include: cytology specimen collection procedure (OTHER), study of high risk factors (PROCEDURE), immunoenzyme technique (OTHER). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT00002667?

This trial is sponsored by Eastern Cooperative Oncology Group, which has 30 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT00002667 being conducted?

This trial has 5 study locations across Florida, Iowa, New Jersey, Ohio, Pennsylvania. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

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