Clinical Trials Directory

Trials / Completed

CompletedNCT01021592

Quality of Life in Multiple Myeloma Patients Treated With Bortezomib

Evaluation of Improvement of Quality of Life in Multiple Myeloma Patients Treated With Velcade (Bortezomib) IV: Prospective, Multicenter, Observational Study

Status
Completed
Phase
Study type
Observational
Enrollment
140 (actual)
Sponsor
Janssen Korea, Ltd., Korea · Industry
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

This observational study will observe the degree of the quality of life in patients with multiple myeloma before and after bortezomib administration by using EORTC-QLQ C30 (European Organization for Research and Treatment of Cancer Quality of Life Questionnaire-Core30) and EQ-5D (EuroQol-5 Dimensions). Both tools are validated research instruments used to measure the quality of life in cancer patients and consequently will provide fundamental data regarding the quality of life in patients with multiple myeloma by analyzing factors that affect the quality of life.

Detailed description

Many clinical studies for the treatment of multiple myeloma have been conducted in Korea, but none of them have evaluated the improvement in the quality of life in patients with multiple myeloma. Most study variables used to evaluate the quality of life of patients with multiple myeloma are subjective and limited. This study will observe the degree of change in the quality of life in patients with multiple myeloma before and after bortezomib administration by using EORTC-C30 (European Organization for Research and Treatment of Cancer Quality of Life Questionnaire-Core30) and EQ-5D (EuroQol-5 Dimensions), validated research instruments used to measure the quality of life in cancer patients and consequently will provide fundamental data regarding the quality of life in patients with multiple myeloma.. Observational Study - No investigational drug administered

Conditions

Interventions

TypeNameDescription
DRUGbortezomibInjection into a vein 1.3 mg/m2 twice a week for 21 days

Timeline

Start date
2007-03-01
Primary completion
2008-07-01
Completion
2008-07-01
First posted
2009-11-30
Last updated
2014-12-23

Source: ClinicalTrials.gov record NCT01021592. Inclusion in this directory is not an endorsement.