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Completed Phase 2 Interventional

Paclitaxel Plus Radiation Therapy in Treating Women With Stage II or Stage III Breast Cancer

ClinicalTrials.gov ID: NCT00006256

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This page only displays public information reproduced from the official ClinicalTrials.gov record NCT00006256. It adds no medical advice, opinions, or eligibility judgments. The official record remains the source of truth for eligibility criteria, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Nov 12, 2026, 7:42 AM EST

All trial information on this site comes from the official ClinicalTrials.gov public API (clinicaltrials.gov/api/v2), run by the U.S. National Library of Medicine. We only display that public information; we do not add opinions, endorsements, or any other intent. Always review the official ClinicalTrials.gov record for the latest information.

Official title

Concurrent Taxol (Paclitaxel) and Definitive Breast Radiation Therapy in Early Stage Breast Cancer Following Four Cycles of Adriamycin/Cytoxan Chemotherapy

Brief summary

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

RATIONALE: Drugs used in chemotherapy use different ways to stop tumor cells from dividing so they stop growing or die. Radiation therapy uses high-energy x-rays to damage tumor cells. Combining paclitaxel with radiation therapy may kill more tumor cells. PURPOSE: This trial is to study the effectiveness of concurrent administration of chemotherapy and radiation therapy in treating women who have stage II or stage III breast cancer by examining the complications and cosmetic effects.

Study identification

NCT ID
NCT00006256
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Enrollment
44 participants

Conditions and interventions

Conditions

Interventions

Drug · Procedure · Radiation

Eligibility (public fields only)

Age range
18 Years to 120 Years
Sex
Female
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
Jun 8, 2000 (Actual)
Primary completion
Nov 30, 2005 (Actual)
Completion
Nov 20, 2023 (Actual)
Last update posted
Nov 30, 2023

2000 – 2023

United States locations

U.S. sites
9
U.S. states
1
U.S. cities
9
Facility City State ZIP Site status
UH-CantonMercy Canton Ohio 44708 —
UH-Geauga Chardon Ohio 44024 —
University Hospitals Cleveland Medical Center, Case Comprehensive Cancer Center Cleveland Ohio 44106-5055 —
UH-Monarch Mayfield Heights Ohio 44124 —
UH-LUICC Mentor Ohio 44060 —
UH-Southwest Middleburg Heights Ohio 44130 —
UH-Chagrin Highlands Orange Ohio 44122 —
UH-Green Road South Euclid Ohio 44121 —
UH-Westlake Westlake Ohio 44145 —

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 NCT00006256, 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 Nov 30, 2023 · Synced Nov 12, 2026

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