NL-OMON47886已完成不适用
Assessing the frequency, phenotype and function of plasmacytoid dendritic cells and T cells in blood and skin of patients with skin fibrosing disorders - Analysis of immune cells in skin fibrosing disorders
niversitair Medisch Centrum Utrecht0 个研究点目标入组 150 人开始时间: 待定最近更新:
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 150
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Observational
入排标准
- 年龄范围
- 18 至 99(—)
入选标准
- •-Age range: 18 - 75 years
- •-Diagnosed with systemic sclerosis, localized scleroderma, eosinophilic fasciitis or psoriasis.
排除标准
- •--Current use of coumarin derivatives
- •-Current use of cyclophosphamide
- •-IV corticosteroids in the last 14 days for inclusion
- •-Age <=17 years
- •-Patients with contra-indications for undergoing a skin biopsy (for example allergic to topical anesthetics)
研究者
相似试验
已完成
不适用
An investigation into the prevalence of MSC and the effectiveness of an intervention program for these patientsPACTR201511000689333Research Directorate, University of the Free State74
尚未招募
不适用
Identification and functional characterization of causal genetic variants in patients with an unexplained bleeding tendencyplaatjesaandoeningenRare bleeding disorders1006447710005330NL-OMON53364Radboud Universitair Medisch Centrum30
招募中
不适用
Functional and structural characterization of the myocardiumdiseases connected to heart failure (e.g. cardiomyopathy)I42CardiomyopathyDRKS00011097niversitätsklinikum Würzburg, Deutsches Zentrum für Herzinsuffizienz50
尚未招募
Unknown
Role of bacteria secreted vesicles in diabetic foot ulcerCTRI/2023/09/057818Science and Engineering research Board (SERB) - Core Research Grant
进行中(未招募)
1 期
Definition of the clinicla manifestation variability, response to treatment and natural history in Pearson and Kearns-Sayre syndromePearson and Kearns-Sayre syndrome.MedDRA version: 20.1Level: PTClassification code 10058799Term: Mitochondrial encephalomyopathySystem Organ Class: 10010331 - Congenital, familial and genetic disordersMedDRA version: 20.1Level: PTClassification code 10051403Term: Mitochondrial DNA deletionSystem Organ Class: 10010331 - Congenital, familial and genetic disordersMedDRA version: 20.0Level: LLTClassification code 10074070Term: Mitochondrial encephalopathySystem Organ Class: 10010331 - Congenital, familial and genetic disordersEUCTR2019-003028-19-ITIRCCS, OSPEDALE PEDIATRICO BAMBINO GESÙ DI ROMA27
