Clinical TrialID 5214

A Randomized Controlled Study of Postoperative Adjuvant Therapy of Uracil-tegafur (UFT) Compared With Cyclophosphamide/Methotrexate/5-fluorouracil (CMF) in Breast Cancer (NSAS-BC)

NCT00152191

Breast Cancer

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Record Fields

Scalar fields from the final clinical_trial record.

Clinical Trial Id
5214
Evidence Id
5214
Core Evidence Id
5214
Source Clinical Trial Id
5196
Herb2 Clinical Trial Id
HBCT005196
Nct Id
NCT00152191
Title
A Randomized Controlled Study of Postoperative Adjuvant Therapy of Uracil-tegafur (UFT) Compared With Cyclophosphamide/Methotrexate/5-fluorouracil (CMF) in Breast Cancer (NSAS-BC)
Status
Completed
Phase
Phase 3
Study Result
No
Study Condition
Breast Cancer
Study Type
Interventional
Study Design
Allocation: RANDOMIZED|Intervention Model: PARALLEL|Masking: NONE|Primary Purpose: TREATMENT
Intervention
DRUG: UFT (uracil, tegafur)|DRUG: cyclophosphamide, methotrexate, and fluorouracil
Intervention Allocation
Randomized
Intervention Model
Parallel
Intervention Mask
Intervention Purpose
Treatment
Gender
Female
Age
Adult, Older_Adult
Enrollment
1300
Outcome Measure
Relapse-free survival, every course for first three courses, then every other course
Sponsor Collaborator
Taiho Pharmaceutical Co., Ltd.
Funded By
INDUSTRY
Location
National Cancer Center, 5-1-1, Tsukiji, chuo-ku, Tokyo, Japan
Other Id
1023001
Start Date
1996-10
Primary Completion Date
2007-10
Completion Date
2008-01
First Posted
2005-09-09
Results First Posted
Last Update Posted
2011-07-07
Study Document
Study Url
https://clinicaltrials.gov/study/NCT00152191
Title Cn
Title En
A Randomized Controlled Study of Postoperative Adjuvant Therapy of Uracil-tegafur (UFT) Compared With Cyclophosphamide/Methotrexate/5-fluorouracil (CMF) in Breast Cancer (NSAS-BC)
Bilingual Status
semi_complete