- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00184834
Quality of Life and Liver Metastases
September 12, 2005 updated by: Radboud University Medical Center
Quality of Life After Surgical Treatment of Colorectal Liver Metastases
An increasing aggressiveness in the surgical approach of colorectal liver metastases is observed.
This seems only justified when, besides prolongation of survival, also the health status of patients is considered.
The aim of this prospective study is to investigate the impact of surgery on health-related quality of life in this specific patient population operated for colorectal liver metastases.Furthermore, as the indications for hepatic resection are broadened and patients with more extensive liver disease are operated on, the chance of non operable disease at laparotomy will increase.
The effects of such an event on HRQol are also studied.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
In a prospective study several patients groups were identified.
Patients undergoing liver resection and/or local ablative therapy.
Patients with non operable disease at (explorative) laparotomy and outpatients with non operable disease as shown during work up for liver resection.
Several validated instruments on HRQoL were ompleted preoperatively (baseline), a half month after operation and then every three months.
Study Type
Observational
Enrollment
100
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
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Nijmegen, Netherlands, 6500 HB
- Radboud University Nijmegen Medical Centre
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
1 second and older (ADULT, OLDER_ADULT, CHILD)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
colorectal liver metastases (operable and non operable disease) and participation by means of filling in quality of life instruments
Exclusion Criteria:
drop out and therefore loss of quality of life instruments
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: Theo Ruers, MD, PhD, Radboud University Medical Center
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
June 1, 1999
Study Completion
November 1, 2002
Study Registration Dates
First Submitted
September 12, 2005
First Submitted That Met QC Criteria
September 12, 2005
First Posted (ESTIMATE)
September 16, 2005
Study Record Updates
Last Update Posted (ESTIMATE)
September 16, 2005
Last Update Submitted That Met QC Criteria
September 12, 2005
Last Verified
September 1, 2005
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- QoL1
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.