Viewing Study NCT01013805


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Study NCT ID: NCT01013805
Status: COMPLETED
Last Update Posted: 2017-07-12
First Post: 2009-10-08
Is Gene Therapy: True
Has Adverse Events: False

Brief Title: Preoperative Radiotherapy and Chemotherapy in Patients With Locally Advanced Rectal Cancer
Sponsor: Trans Tasman Radiation Oncology Group
Organization:

Study Overview

Official Title: A Phase II Trial of Integrated Preoperative Radiotherapy and Chemotherapy With Oxaliplatin 5-FU and Folinic Acid in Patients With Locally Advanced Rectal Cancer
Status: COMPLETED
Status Verified Date: 2017-07
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: PROArCT
Brief Summary: The aims of the trial are (1) to determine the tolerability rate in the setting of a multi-centre study and (2) to determine secondary tolerability endpoints, toxicity rates and complete pathologic response rate in patients with locally advanced rectal cancer who are treated with an integrated preoperative radiotherapy with FOLFOX chemotherapy regimen.
Detailed Description: None

Study Oversight

Has Oversight DMC: False
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?:

Secondary ID Infos

Secondary ID Type Domain Link View
ACTRN12610000175077 REGISTRY Australia New Zealand Clinical Trials Registry View