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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02708732
Other study ID # ML29956
Secondary ID
Status Completed
Phase N/A
First received March 10, 2016
Last updated April 19, 2017
Start date May 31, 2016
Est. completion date October 31, 2016

Study information

Verified date April 2017
Source Hoffmann-La Roche
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

This study is a prospective, cross-sectional survey to be administered to real patients in remission from DLBCL using a 15-minute postal or online survey. The project is designed to describe the impact of DLBCL remission on health utility and quality of life. Data collection will occur over a 4-month period.


Recruitment information / eligibility

Status Completed
Enrollment 91
Est. completion date October 31, 2016
Est. primary completion date October 31, 2016
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Adults greater than or equal to (>/=) 18 years of age

- Diagnosis of DLBCL and currently in first remission

- Prior drug treatment for DLBCL

Exclusion Criteria:

- Receiving active treatment for DLBCL

- Relapsed following any treatment for DLBCL

Study Design


Locations

Country Name City State
United Kingdom PH Associates - an OPen Health Company Marlow

Sponsors (1)

Lead Sponsor Collaborator
Hoffmann-La Roche

Country where clinical trial is conducted

United Kingdom, 

Outcome

Type Measure Description Time frame Safety issue
Primary Health-Related Quality of Life According to European Quality of Life 5-Dimension 5-Level (EQ-5D-5L) Score Up to 4 months of data collection
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