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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02033928
Other study ID # OSU-13135
Secondary ID
Status Completed
Phase N/A
First received December 18, 2013
Last updated February 27, 2018
Start date April 2014
Est. completion date August 2017

Study information

Verified date February 2018
Source Ohio State University Comprehensive Cancer Center
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The purpose of this research study is to describe a patients' fitness before and after treatment (whether that treatment be chemotherapy or a transplant). Fitness is a way of measuring a patient's current quality of health. With surveys, questionnaires and blood tests, we hope to create a tool that will give a good picture of patients' ability to tolerate treatment. In the future, we hope to devise the best treatment for a patient based on their "fitness".


Recruitment information / eligibility

Status Completed
Enrollment 111
Est. completion date August 2017
Est. primary completion date August 2017
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- patients with a plasma cell dyscrasia AND/OR any patient receiving a stem cell transplant for a hematologic malignancy at The Ohio State University

- at least 18 years of age

Exclusion Criteria:

- Any medical or psychiatric condition that would make it difficult for the patient to comply with study procedures.

Study Design


Locations

Country Name City State
United States The Ohio State University Hospital East Columbus Ohio

Sponsors (1)

Lead Sponsor Collaborator
Ohio State University Comprehensive Cancer Center

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Other Overall survival We will assess overall survival and the relationship of those measures to patients' functional, cognitive and psychosocial health. enrollment to date of death up to two years post-enrollment
Primary Change in Comprehensive Frailty Assessment Responses to the Comprehensive Frailty Assessment will be assessed before and after treatment and changes will be evaluated. In transplant patients, this will be measured one year post transplant and in the non-transplant arm, this will be assessed after the second cycle of treatment. up to 14 months
Secondary Time to progression We will assess time to progression for multiple myeloma patients and the relationships of those outcomes to patients' functional, cognitive and psychosocial health. date of enrollment to date of documented clinical progression up to two years post-enrollment
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