NIPH Clinical Trials Search

JAPANESE
国立保健医療科学院
UMIN ID: UMIN000001446

Registered date:21/10/2008

Dose-escalation study of adjuvant vinorelbine plus cisplatin with Japanese completely resected stage I-IIIA non-small-cell lung cancer

Basic Information

Recruitment status Complete: follow-up complete
Health condition(s) or Problem(s) studiedPatients with completely resected non-small-cell lung cancer with stage IB-IIIA and stage IA with 2cm or more
Date of first enrollment2008/06/01
Target sample size9
Countries of recruitmentJapan
Study typeInterventional
Intervention(s)Level 1: Vinorelbin (20mg/m2)+Cisplatin (40mg/m2) Level 2: Vinorelbin (25mg/m2)+Cisplatin (40mg/m2) Level 3: Vinorelbin (25mg/m2)+Cisplatin (45mg/m2)

Outcome(s)

Primary OutcomeMaximum tolerance dose
Secondary Outcome

Key inclusion & exclusion criteria

Age minimum18years-old
Age maximumNot applicable
GenderMale and Female
Include criteria
Exclude criteria1.inadequate conditon for chemotherapy 2.Patients with a histoly of concurrent malignancy sidease were excluded

Related Information

Contact

public contact
Name Kazuhito Funai
Address Japan
Telephone
E-mail kfunai@hmedc.or.jp
Affiliation Hamamatsu Medicar Cencer Thoracic surgery
scientific contact
Name Shigeru Momiki
Address 328, Tomiduka, Naka, Hamamatsu, Shizuoka, Japan Japan
Telephone
E-mail
Affiliation Hamamatsu medicar cencer Division of Thoracic Surgery