Assessment of Interleukin-4 Tissue and Serum Levels in Pityriasis Lichenoides Chronica Patients : a Case- Control Study
| Registry | NCT06889506 |
|---|---|
| Status | Not yet recruiting |
| Phase | Not applicable |
| Study type | Interventional; non randomized, parallel, masking: none, diagnostic |
| Enrollment | 50 (Estimated) |
| Sponsor | Cairo University (Other) |
| Conditions | Pityriasis Lichenoides |
| Interventions | skin biopsy and serum sample (Procedure) |
| Dates | start 2025-04-01 (estimated), primary completion 2025-07-01 (estimated), completion 2025-07-01 (estimated), first posted 2025-03-21, last updated 2025-03-21 |
Related Papers Related Patents Related Grants Related Experts
All trials for Pityriasis Lichenoides All trials of skin biopsy and serum sample
assessment of the level of interleukin 4 (IL-4) in the lesional skin and serum of PLC patients and compare its level with healthy controls.
measuring the level of Interleukin 4 in lesional skin and it's serum level using ELIZA in patients with Pityriasis lichenoides chronica and comparing the levels with healthy controls levels
| Arm | Type | Interventions | Description |
|---|---|---|---|
| PLC patients | Active comparator | Procedure: skin biopsy and serum sample | one skin biopsy (lesional) and serum sample will be taken from every patient |
| healthy controls | Experimental | Procedure: skin biopsy and serum sample | a skin biopsy and serum sample will be taken from each control sample |
Sex: All, ages: 18 Years to any, accepts healthy volunteers
Inclusion Criteria: * Patients with pityriasis lichenoides Chronica (PLC): either with the classical presentation papular or hypo-pigmented macules and patches that proved histopathologically to be PLC. * Both genders * Age group ≥ 8 years Exclusion Criteria: * Patients with other skin diseases * Patient received treatment for PLC within period less than three months * Pregnant patients * Lactating patients