Serum Interleukin -21 Level in Patients With Severe Adverse Cutaneous Drug Reaction.
NCT ID: NCT03166241
Last Updated: 2017-05-25
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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UNKNOWN
NA
30 participants
INTERVENTIONAL
2017-07-31
2018-12-31
Brief Summary
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Detailed Description
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Steven-Johnson syndrome (SJS) and Toxic Epidermal Necrolysis (TEN) are considered a spectrum of acute life-threatening mucocutaneous reactions that differ only in severity. Both diseases are characterized by mucous membrane and skin involvement, are often caused by medications and are collectively known as epidermal necrolysis or scalded skin syndrome.Stevens-Johnson syndrome (SJS) is classified as an epidermal loss \<10% of the body surface area.Toxic Epidermal Necrolysis (TEN) is indicated by \>30% body surface area erosion. The range of epidermal loss between 10% and 30% is called Stevens-Johnson syndrome-Toxic Epidermal Necrolysis (SJS-TEN) overlap. Severity of illness score \[Score of Toxic Epidermal Necrolysis(TEN) \] has been devised to predict prognosis in patients with Epidermal Necrolysis.This scoring system addresses 7 prognostic factors: age, malignancy, heart rate,Body Surface Area involved, serum urea, serum glucose and serum bicarbonate levels.
Interleukin-21 regulates both innate and adaptive immune responses and it is not only has key roles in antitumour and antiviral responses that promote the development of autoimmune diseases and inflammatory disorders. It is recently discovered member of the type 1 cytokine family which is produced by activated clusters of differentiation 4+ T cells ,Natural killer cells and follicular helper T cells.
Conditions
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Study Design
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RANDOMIZED
PARALLEL
DIAGNOSTIC
NONE
Study Groups
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study group
measure serum interleukin 21 level in patients with severe adverse drug reaction who show change in serum interleukin 21 before and after therapy the following investigation will be done at the begning of the study to patients: Complete Blood Picture Erythrocyte Sedimentation Rate Random blood sugar Liver function tests Kidney function tests
serum interleukin 21
it is cytokine used as a marker to detect it's level in patients with adverse drug reactions
Complete Blood Picture
It is a blood sample will taken from patients to detect any abnormalities in blood component at the start of the study
Liver function test
It is a blood sample will taken from patients to detect any associated liver disease at the start of the study
Random Blood Sugar
measure blood sugar in patients included in the study at the start of the study
Erythrocyte Sedimentation Rate
blood sample will be taken from patients to detect any abnormalities in erythrocyte sedimentation rate at the start of the study
Kidney function tests
blood sample will be taken from patients to detect any kidney disease before the start of the study
control group
compare serum interleukin 21 level in patients with severe adverse drug reaction and healthy control subjects
serum interleukin 21
it is cytokine used as a marker to detect it's level in patients with adverse drug reactions
Interventions
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serum interleukin 21
it is cytokine used as a marker to detect it's level in patients with adverse drug reactions
Complete Blood Picture
It is a blood sample will taken from patients to detect any abnormalities in blood component at the start of the study
Liver function test
It is a blood sample will taken from patients to detect any associated liver disease at the start of the study
Random Blood Sugar
measure blood sugar in patients included in the study at the start of the study
Erythrocyte Sedimentation Rate
blood sample will be taken from patients to detect any abnormalities in erythrocyte sedimentation rate at the start of the study
Kidney function tests
blood sample will be taken from patients to detect any kidney disease before the start of the study
Eligibility Criteria
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Inclusion Criteria
* Patients with definite drug history.
* Both sex will be included.
Exclusion Criteria
* Patients within 4 weeks of the study.
* Patients receiving phototherapy within 6 months of the study.
* Diabetic patients
* Anaemic patients
* Thyroid disorders,
* Chronic liver or Renal diseases
* Atopy and Parathyroid disorders.
* Patients with known autoimmune diseases or cancer.
* Pregnant or lactating womens.
ALL
No
Sponsors
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Assiut University
OTHER
Responsible Party
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MAHanna
Principal Investigator
Central Contacts
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References
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Farshchian M, Ansar A, Zamanian A, Rahmatpour-Rokni G, Kimyai-Asadi A, Farshchian M. Drug-induced skin reactions: a 2-year study. Clin Cosmet Investig Dermatol. 2015 Feb 9;8:53-6. doi: 10.2147/CCID.S75849. eCollection 2015.
Hidajat C, Loi D. Drug-mediated rash: erythema multiforme versus Stevens-Johnson syndrome. BMJ Case Rep. 2014 Sep 22;2014:bcr2014205543. doi: 10.1136/bcr-2014-205543.
Ellender RP, Peters CW, Albritton HL, Garcia AJ, Kaye AD. Clinical considerations for epidermal necrolysis. Ochsner J. 2014 Fall;14(3):413-7.
Gong F, Su Q, Pan YH, Huang X, Shen WH. The emerging role of interleukin-21 in allergic diseases (Review). Biomed Rep. 2013 Nov;1(6):837-839. doi: 10.3892/br.2013.166. Epub 2013 Sep 12.
Other Identifiers
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ACDR
Identifier Type: -
Identifier Source: org_study_id
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