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Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT00208936
Other study ID # 0691-1995
Secondary ID
Status Terminated
Phase Phase 2
First received September 13, 2005
Last updated September 5, 2014
Start date January 1996

Study information

Verified date September 2014
Source Emory University
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Interventional

Clinical Trial Summary

This study is designed pre-operative for patients with resectable, local-regional carcinoma of the esophagus.


Description:

This study is designed for patients with resectable, local-regional carcinoma of the esophagus. In a pre-operative setting, chemotherapy with Taxol, Cisplatin, and 5-Fluorouracil will be administered followed by G-CSF.


Recruitment information / eligibility

Status Terminated
Enrollment 20
Est. completion date
Est. primary completion date March 2006
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Measurable disease with resectable local-regional carcinoma of the esophagus. 18 years of age or older.

Exclusion Criteria:

- Pregnant or lactating. Non-resectable local-regional carcinoma of the esophagus.

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Drug:
Taxol, Cisplatin, 5-Fluorouracil, G-CSF


Locations

Country Name City State
United States Emory University Winship Cancer Institute Atlanta Georgia

Sponsors (1)

Lead Sponsor Collaborator
Emory University

Country where clinical trial is conducted

United States, 

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