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Informative Value of Determining the Level of NF-κB Translocation in Lymphocyte Populations in Children With Psoriasis

Primary Purpose

Psoriasis Vulgaris

Status
Completed
Phase
Not Applicable
Locations
Russian Federation
Study Type
Interventional
Intervention
Peripheral blood samples were obtained following the standard procedures.
Sponsored by
National Medical Research Center for Children's Health, Russian Federation
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Psoriasis Vulgaris focused on measuring NF-κB translocation, Lymphocytes, Flow cytometry with imaging (Amnis), Biological drugs, Сhildren and adolescents

Eligibility Criteria

1 Year - 18 Years (Child, Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  1. Age from 1 to 18 years old
  2. Mild, moderate, and severe psoriasis
  3. Healthy children, as a comparison group
  4. Patients receiving basic and external therapy, receiving systemic therapy with methotrexate and patients receiving therapy with biological drugs (Adalimumab, Etanercept, Ustekinumab)
  5. A signed and dated informed consent received from the patient's parents (guardians), as well as from a patient over 14 years of age, to participate in the study
  6. Ability to attend control visits within the specified time frame

Exclusion Criteria:

  1. The presence of other concomitant skin diseases in the present or in the past, which could affect the assessment of the effect of the study drugs on the course of psoriasis
  2. Use of other genetically engineered biological preparations in therapy
  3. Participation in other clinical trials
  4. Extensive or complete disability, significantly limiting personal care or determining the inability to carry it out
  5. Immunodeficiency disease
  6. The presence in the past or present of any serious and / or unstable concomitant disease
  7. The course of a viral, bacterial, fungal or parasitic infection

Sites / Locations

  • National Medical Research Center for Children's Health

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Experimental

Experimental

Arm Label

Level of NF-κB translocation in lymphocyte in children with psoriasis and in comparison group

Level of NF-κB translocation in lymphocyte in children with psoriasis, based on the type of therapy

Severity of psoriasis based on level of NF-κB translocation in psoriasis who received biologics

Arm Description

The analysis of the relative count of cells with NF-κB translocation in the lymphocyte populations the group of patients with psoriasis and in the comparison group.

Determination of the level of NF-kB translocation in lymphocyte populations in patient groups depending on the type of therapy: Group 1 - patients receiving basic and external therapy; Group 2 - patients receiving methotrexate; and Group 3 - patients receiving therapy with biological drugs.

Assessment of the level of NF-kB translocation in lymphocyte populations, assessment of PASI and BSA, assessment of the effectiveness of biological drugs in patients with psoriasis. Identification of patients in the stage of regression of the disease and in the progressive stage.

Outcomes

Primary Outcome Measures

The level of NF-kB translocation in lymphocyte populations
Changes in NF-kB translocation in lymphocyte populations
Patient age
Age assessment
PASI (Psoriasis Area Severity Index)
Change of the PASI
BSA (Body Surface Area)
Assessment of the affected area of the patient's body

Secondary Outcome Measures

Full Information

First Posted
July 26, 2021
Last Updated
August 3, 2021
Sponsor
National Medical Research Center for Children's Health, Russian Federation
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1. Study Identification

Unique Protocol Identification Number
NCT04989296
Brief Title
Informative Value of Determining the Level of NF-κB Translocation in Lymphocyte Populations in Children With Psoriasis
Official Title
Informative Value of Determining the Level of NF-κB Translocation by Flow Cytometry With Visualization in Lymphocyte Populations in Children With Psoriasis
Study Type
Interventional

2. Study Status

Record Verification Date
July 2021
Overall Recruitment Status
Completed
Study Start Date
September 1, 2018 (Actual)
Primary Completion Date
November 20, 2019 (Actual)
Study Completion Date
January 15, 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
National Medical Research Center for Children's Health, Russian Federation

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
This study is the first to quantify the level of NF-kB translocation in lymphocyte populations in children and adolescents with psoriasis of varying severity.
Detailed Description
This is a diagnostic study aimed at finding immunological predictors of the effectiveness of therapy in children and adolescents with psoriasis. The study included 90 patients from 1 to 18 years old with psoriasis vulgaris, mild / moderate and severe. The comparison group consisted of 30 healthy children. The study took into account the PASI (Psoriasis Area Severity Index); the BSA (Body Surface Area); including patient age; duration of the disease; type of therapy; duration of therapy. Depending on the type of therapy, all psoriatic children were divided into 3 groups: Group 1 (n = 24) - patients receiving basic and external therapy; Group 2 (n = 20) - patients receiving systemic therapy with methotrexate; and Group 3 (n = 46) - patients receiving therapy with genetically engineered biological drugs (Adalimumab, Etanercept, Ustekinumab). The analysis of the NF-κB translocation level in lymphocytes was performed by flow cytometry with imaging (Image Stream Mark II - AMNIS) using the Amnis NF-κB Translocation Kit.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Psoriasis Vulgaris
Keywords
NF-κB translocation, Lymphocytes, Flow cytometry with imaging (Amnis), Biological drugs, Сhildren and adolescents

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Non-Randomized
Enrollment
120 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Level of NF-κB translocation in lymphocyte in children with psoriasis and in comparison group
Arm Type
Experimental
Arm Description
The analysis of the relative count of cells with NF-κB translocation in the lymphocyte populations the group of patients with psoriasis and in the comparison group.
Arm Title
Level of NF-κB translocation in lymphocyte in children with psoriasis, based on the type of therapy
Arm Type
Experimental
Arm Description
Determination of the level of NF-kB translocation in lymphocyte populations in patient groups depending on the type of therapy: Group 1 - patients receiving basic and external therapy; Group 2 - patients receiving methotrexate; and Group 3 - patients receiving therapy with biological drugs.
Arm Title
Severity of psoriasis based on level of NF-κB translocation in psoriasis who received biologics
Arm Type
Experimental
Arm Description
Assessment of the level of NF-kB translocation in lymphocyte populations, assessment of PASI and BSA, assessment of the effectiveness of biological drugs in patients with psoriasis. Identification of patients in the stage of regression of the disease and in the progressive stage.
Intervention Type
Diagnostic Test
Intervention Name(s)
Peripheral blood samples were obtained following the standard procedures.
Intervention Description
Taking 4 ml of peripheral blood from patients on an empty stomach.
Primary Outcome Measure Information:
Title
The level of NF-kB translocation in lymphocyte populations
Description
Changes in NF-kB translocation in lymphocyte populations
Time Frame
Screening on the 1 day of blood sampling
Title
Patient age
Description
Age assessment
Time Frame
from 1 to 18 years old
Title
PASI (Psoriasis Area Severity Index)
Description
Change of the PASI
Time Frame
1 day Screening at the time of examination
Title
BSA (Body Surface Area)
Description
Assessment of the affected area of the patient's body
Time Frame
1 day Screening at the time of examination

10. Eligibility

Sex
All
Minimum Age & Unit of Time
1 Year
Maximum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Age from 1 to 18 years old Mild, moderate, and severe psoriasis Healthy children, as a comparison group Patients receiving basic and external therapy, receiving systemic therapy with methotrexate and patients receiving therapy with biological drugs (Adalimumab, Etanercept, Ustekinumab) A signed and dated informed consent received from the patient's parents (guardians), as well as from a patient over 14 years of age, to participate in the study Ability to attend control visits within the specified time frame Exclusion Criteria: The presence of other concomitant skin diseases in the present or in the past, which could affect the assessment of the effect of the study drugs on the course of psoriasis Use of other genetically engineered biological preparations in therapy Participation in other clinical trials Extensive or complete disability, significantly limiting personal care or determining the inability to carry it out Immunodeficiency disease The presence in the past or present of any serious and / or unstable concomitant disease The course of a viral, bacterial, fungal or parasitic infection
Facility Information:
Facility Name
National Medical Research Center for Children's Health
City
Moscow
ZIP/Postal Code
119296
Country
Russian Federation

12. IPD Sharing Statement

Plan to Share IPD
Undecided

Learn more about this trial

Informative Value of Determining the Level of NF-κB Translocation in Lymphocyte Populations in Children With Psoriasis

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