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NCT03197259 Clinical Trial

Chronic Lymphocytic Leukemia Registry Study - Multicenter Prospective National Study

Chronic Lymphocytic Leukemia Clinical Trial

— CLLTRegistry  

Official title:
Turkish Chronic Lymphocytic Leukemia Study Group Registry - Multicenter Prospective Study

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT03197259
Other study ID # CLL TR Registry
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date January 1, 2017
Est. completion date August 1, 2026

Study information
Verified date March 2021
Source Izmir Hematologic Diseases and Cancer Research Help Association
Contact Fatih Demirkan, Prof
Phone +90 542 515 17 80
Email fatihdemirkan@yahoo.com
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

A prospective, multicenter national observational study for patients diagnosed as chronic lymphocytic leukemia across 25 centers in Turkey

Description:

The purpose of this study is to explore the history and real world management of patients diagnosed with CLL, provide insight into the management of CLL, and evaluate the effectiveness of first, second and subsequent therapeutic strategies employed in both the community and academic settings.

Recruitment information / eligibility
Status Recruiting
Enrollment 1000
Est. completion date August 1, 2026
Est. primary completion date January 1, 2023
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Patients diagnosed as CLL - 18 years or older - Able and willing to provide the written informed consent Exclusion Criteria: - Younger than 18 years

Study Design

Related Conditions & MeSH terms

Locations
Country Name City State
Turkey Dokuz Eylum Medical Favulty Izmir

Sponsors (1)
Lead Sponsor Collaborator
Fatih Demirkan, MD

Country where clinical trial is conducted

Turkey, 

Outcome
Type Measure Description Time frame Safety issue
Primary First line therapy therapy protocol distrubition The primary objective is to describe percentage of first line therapy protocols in patients initiated on therapy for CLL in the community and academic setting 36 months
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