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Surgical Procedures for Advanced Tumor Disease. A Prospective Study Evaluating Quality of Life

NCT01367795 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 26

Last updated 2015-03-27

No results posted yet for this study

Summary

Patients in a known palliative setting and with localized symptoms due to tumor growth will be evaluated for their quality of life before and after a surgical intervention (primary endpoint). Medical outcome in terms of length of stay in hospital, length of stay on a intensive care unit, complications, reinterventions will be recorded (secondary endpoints). The investigators will also observe patients with conservative treatment.

Conditions

Sponsors & Collaborators

  • Kantonsspital Olten

    collaborator OTHER

  • University Hospital, Basel, Switzerland

    lead OTHER

Principal Investigators

  • Carsten T. Viehl, MD · Department of Surgery, University Hospital of Basel

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2010-07-31
Primary Completion
2014-10-31
Completion
2014-10-31

Countries

  • Switzerland

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01367795 on ClinicalTrials.gov