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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01397916
Other study ID # CLL-IDO
Secondary ID
Status Completed
Phase
First received
Last updated
Start date February 2010
Est. completion date December 2010

Study information

Verified date February 2022
Source Tampere University Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The Activity of Indoleamine 2,3-dioxygenase in patients with Chronic Lymphocytic Leukemia (CLL) is studied.


Description:

The Activity of Indoleamine 2,3-dioxygenase in patients with Chronic Lymphocytic Leukemia (CLL)is studied in patients and healthly controls.


Recruitment information / eligibility

Status Completed
Enrollment 73
Est. completion date December 2010
Est. primary completion date December 2010
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 15 Years to 85 Years
Eligibility Inclusion Criteria: - Patients with CLL and lymphocyte count > 10 x 109/l Exclusion Criteria: - Acute infection

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
Finland Tampere university Hospital Tampere

Sponsors (1)

Lead Sponsor Collaborator
Tampere University Hospital

Country where clinical trial is conducted

Finland, 

Outcome

Type Measure Description Time frame Safety issue
Primary IDO activity and expression measured by kynurenine/tryptophan ratio in serum and by PCR in peripheral blood mononuclear cells. Indoleamine 2,3 -dioxygenase (IDO) activity in patients with CLL was measured by the serum kynurenine/tryptophan (kyn/trp) ratio and - the expression of INDO (encoding IDO enzyme) and INDOL1 (encoding IDO2 enzyme) genes in peripheral blood mononuclear cells via TaqMan real-time PCR. 3 months
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