World Health Organization site
Skip Navigation Links

Main
Note: This record shows only the 20 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register.
Register: KCT
Last refreshed on: 27 April 2013
Main ID:  KCT0000287
Date of registration: 12/12/2011
Primary sponsor: SEOUL NATIONAL UNIVERSITY HOSPITAL
Public title: ARFI elastography for the prediction of chemotherapeutic response in the patient with metastatic liver lesions
Scientific title: ARFI elastography for the prediction of chemotherapeutic response in the patient with metastatic liver lesions
Date of first enrolment: 2009-12-24
Target sample size: 46
Recruitment status: Recruiting
URL:  http://cris.nih.go.kr/cris/en/search/search_result_st01.jsp?seq=1681
Study type:  Interventional Study
Study design:  Primary Purpose : Diagnostic, Intervention Model : Single Group, Blinding/Masking : Open, Allocation : Not Applicable  
Countries of recruitment
Korea, Republic of
Contacts
Name: Jae Young  Lee
Address: 
Telephone:
Email:
Affiliation:  SEOUL NATIONAL UNIVERSITY HOSPITAL
Name: Soo Yeoun  Kang
Address: 
Telephone:
Email:
Affiliation:  SEOUL NATIONAL UNIVERSITY HOSPITAL
Key inclusion & exclusion criteria
Inclusion criteria: 1. Being diagnosed as liver metastasis newly, planned chemotherapy for the first time or changed other chemotheraphy
2. tumor should be measurable by CT or MR
3. tumor should be measurable by ARFI elastography

Exclusion criteria: 1. not cooperative
2. the presence of ascites
3. difficulty in communication


Age minimum: N/A(No Limit)
Age maximum: N/A(No Limit)
Gender: Both
Health Condition(s) or Problem(s) studied
Neoplasms
Intervention(s)
Device : total 6 times Ultrasonography; before chemotherapy, 48Hr after chemotherapy starting, 1week, 2week, 3week,4week
Primary Outcome(s)
The difference of ARFI average values between response and nonresponse group after chemotherapy
Secondary Outcome(s)
The time when the difference of ARFI value between response and nonresponse group becomes statistically significant.
Secondary ID(s)
Source(s) of Monetary Support
Secondary Sponsor(s)
SEOUL NATIONAL UNIVERSITY HOSPITAL
Disclaimer: Trials posted on this search portal are not endorsed by WHO, but are provided as a service to our users. In no event shall the World Health Organization be liable for any damages arising from the use of the information linked to in this section. None of the information obtained through use of the search portal should in any way be used in clinical care without consulting a physician or licensed health professional. WHO is not responsible for the accuracy, completeness and/or use made of the content displayed for any trial record.
Copyright - World Health Organization - Version 3.1 - Version history