- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00871520
Prognosis and Survival Estimates in Palliative Therapy
August 22, 2016 updated by: Heinrich-Heine University, Duesseldorf
Prognosis in Palliative Therapy - a Prospective Study on Survival Prognostication in Advanced Stage Cancer Patients
The accuracy of clinical survival estimates is tested in comparison to objective prognostic scores.
Study Overview
Detailed Description
- At presentation a clinical survival estimate is obtained in each patient.
- Survival is also estimated using published prognostic scores in palliative care.
- Prognostic scores based on blood samples, general symptoms, complaints, and performance status are calculated and validated, respectively
- Each patient completes questionnaires on psychological distress
- Survival estimates are limited to 6 months.
- Each patient is followed for at least 6 months.
Study Type
Observational
Enrollment (Actual)
612
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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NRW
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Duesseldorf, NRW, Germany, 40225
- University Hospital Duesseldorf, Radiation Oncology Dept.
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Duesseldorf, NRW, Germany, 40593
- Sana Kliniken Duesseldorf Benrath
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Duesseldorf, NRW, Germany, 40625
- Sana Kliniken Duesseldorf Gerresheim, MVZ Onkologie
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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
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
Consecutive unselected cancer patients referred for palliative treatment to one of the participating institutions.
Description
Inclusion Criteria:
- oncologic disease confirmed
- incurable locally advanced or metastatic disease
- palliative treatment intended
- age > 18
- able to understand the study protocol
- able to complete the forms with assistance if necessary
Exclusion Criteria:
- therapy with curative intent
- regular clinical follow-up visit without disease progression
- ongoing therapy
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
- Observational Models: Cohort
- Time Perspectives: Prospective
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
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Palliative Therapy
Patients referred to the oncology / radiation oncology departments for palliative therapy.
|
There are no specific interventions in this observational study
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Survival
Time Frame: 6 months
|
6 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: Stephan Gripp, Dr., Universtity Hospital Duesseldorf, Radiation Oncology Department
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
April 1, 2008
Primary Completion (Actual)
December 1, 2011
Study Completion (Actual)
August 1, 2016
Study Registration Dates
First Submitted
March 27, 2009
First Submitted That Met QC Criteria
March 27, 2009
First Posted (Estimate)
March 30, 2009
Study Record Updates
Last Update Posted (Estimate)
August 23, 2016
Last Update Submitted That Met QC Criteria
August 22, 2016
Last Verified
August 1, 2016
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- Pro-08
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.