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Clinical Trials/NCT05092048
NCT05092048
Unknown
Not Applicable

Validation Value of the Questionnaire to Assess Health-related Quality of Life in Patients With CML

xuna1 site in 1 country10,000 target enrollmentSeptember 22, 2021

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
CML (Chronic Myelogenous Leukemia)
Sponsor
xuna
Enrollment
10000
Locations
1
Primary Endpoint
Assess health-related Quality of Life and Symptom Burden in patients with chronic myeloid leukemia
Last Updated
4 years ago

Overview

Brief Summary

Successful outcomes in CML require both prolonged adherence to oral TKI therapy by patients and careful monitoring of treatment responses by their physicians. Patient Reported Outcomes(PRO) assessment is important to facilitate decisions in the current treatment landscape of CML.

Detailed Description

1. Above 18 years of age. 2. Patient with confirmed diagnosis of Philadelphia chromosome positive and/or BCR-ABL positive chronic myeloid leukemia (CML). 3. Written informed consent. 4. Patients enrolled in investigational drug-trials or other type of clinical trials are also eligible.

Registry
clinicaltrials.gov
Start Date
September 22, 2021
End Date
October 1, 2022
Last Updated
4 years ago
Study Type
Observational

Investigators

Sponsor
xuna
Responsible Party
Sponsor Investigator
Principal Investigator

xuna

professor

Nanfang Hospital, Southern Medical University

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Assess health-related Quality of Life and Symptom Burden in patients with chronic myeloid leukemia

Time Frame: 1 year

Health-related quality of life (HRQOL) assessment in the current treatment landscape of chronic myeloid leukemia

Study Sites (1)

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