Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-24 @ 7:55 PM
Ignite Modification Date:
2025-12-24 @ 7:55 PM
NCT ID:
NCT02553304
Eligibility Criteria:
Inclusion Criteria:
1. Patients with confirmed diagnosis of CLL, either histologically proven or with immunophenotypical pattern by flowcytometry
2. The diagnosis of CLL was made after 2000; the complete medical history and the laboratory data are available for collections.
3. Age of 20 or older
4. Willing to cooperate with the informed consent procedure and the collections of blood samples and medical history.
5. There are no limitations about organ functions, performance status, pregnancy or breast feeding status, or concomitant diseases or medicines.
6. The patient's peripheral hemogram shows apparent leukocytosis (\>15 k/μL) with lymphocytosis (lymphocytes+atypical lymphocytes \>55%); the data should me within 3 months before study enrollment.
Exclusion Criteria:
1. The patient's past history, including the diagnostic test results, the prior CLL-related treatment courses, the drug history, et.al, is not available.
2. The patient cannot complete the informed consent procedures.
3. The diagnosis is T-CLL, or the patients have been in complete remission without peripheral leukemia cells.
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
20 Years
Study:
NCT02553304
Study Brief:
Protocol Section:
NCT02553304