The Role of interferOn and Complement in SecondAry thRombotic micrioangiOpathy (ROSARIO)
The Role of interferOn and Complement in SecondAry thRombotic micrioangiOpathy (ROSARIO)
Study rationale: Viral infections, such as CMV, are a risk factor for TA-TMA (transplantation-associated TMA). Viral infections increase interferon (IFN) levels and high IFN levels are associated with thrombotic microangiopathy (TMA). IFNs contribute to TMA pathogenesis through suppression of VEGF transcription. Disruption of the VEGF signalling pathway in the kidney is associated with TMA.
Primary objective: To determine the association between IFN levels and the development of biopsy-proven or clinically diagnosed TA-TMA.
Secondary objective(s): To explore the relationship between complement activation and IFN in patients with TMA.
To explore if high IFN levels are associated with low VEGF-A levels. Endpoint: The study aims to investigate the role of IFN in the pathogenesis of secondary thrombotic microangiopathy (focusing on patients with TA-TMA). It seeks to clarify whether IFN, next to complement dysregulation, is a driver of endothelial damage and TMA in these patients.
연구 개요
상태
상태
정황
정황
개입 / 치료
개입 / 치료
연구 유형
연구 유형
등록 (추정된)
등록
단계
단계
- 해당 없음
연락처 및 위치
연구 연락처
연구 연락처
- 이름: Sofie A Dhaese, MD, PhD
- 전화번호: +320050452200
- 이메일: sofie.dhaese@azsintjan.be
참여기준
자격 기준
자격 기준
공부할 수 있는 나이
- 성인
- 고령자
건강한 자원 봉사자를 받아들입니다
설명
Inclusion Criteria:
Participants eligible for inclusion in this study must meet all of the following criteria:
- Voluntary written informed consent of the participant or their legally authorized representative has been obtained prior to any screening procedures
- At least 18 years of age at the time of signing the Informed Consent Form (ICF)
Specifically for the patients with TMA (G1 and G4):
- Patients after allogeneic or autologous hematopoietic stem cell transplantation (HSCT) OR patients after solid organ transplantation OR patients with DITMA AND
- Tissue diagnosis of TMA (pathological diagnosis) OR
Clinical diagnosis of TMA based on the following criteria, with ≥4 out of 6 features fulfilled within 14 days (15,52,53):
de novo Coombs negative hemolytic anemia OR (in case of HSCT)
- failure to achieve transfusion independence despite neutrophil engraftment
- hemoglobin decline by ≥ 1g/dL
- new onset transfusion dependence
otherwise unexplained de novo thrombocytopenia (< 50 x 109/L) OR a 25% decrease in platelet count OR (in case of HSCT)
- failure to achieve platelet engraftment despite neutrophil engraftment
- higher than expected transfusion needs
- refractory to platelet transfusion *≥50% reduction in platelet count after full platelet engraftment
- lactate dehydrogenase (LDH) above the upper limit of normal
- schistocytes (=>2 / high power field (HPF)
- new onset hypertension OR worsening of existing hypertension requiring additional antihypertensive therapy
- proteinuria > 1g/g creatinine on a random urine protein-to-creatinine ratio Date of TMA diagnosis = first date when ≥4 out of the 6 features are fulfilled.
Specifically for the group of patients without TMA, with infection (G2):
- Patients after allogeneic or autologous hematopoietic stem cell transplantation (HSCT) OR patients after solid organ transplantation AND
- Symptomatic viral infection (evaluated by the treating physician).
Specifically for the group of patients without TMA, without infection (G3):
- Patients after allogeneic or autologous hematopoietic stem cell transplantation (HSCT) OR patients after solid organ transplantation AND
- No symptomatic viral infection (evaluated by the treating physician).
Exclusion Criteria:
Participants eligible for this study must not meet any of the following criteria:
- Participant has a personal or family history of aHUS
- Participant has a history of malignant hypertension
- Participant has a history of active cancer, excluding the haematological cancer for which the patient received the stem cell transplantation (if applicable)
- The participant received prior complement inhibition
- The participant received prior anti-interferon treatment
- If applicable: Female who is pregnant, breast-feeding or intends to become pregnant the following year or is of child-bearing potential and not using an adequate, highly effective contraceptive
- Participation in an interventional study with an investigational medicinal product (IMP) or device
공부 계획
연구는 어떻게 설계됩니까?
디자인 세부사항
- 주 목적: 치료
- 할당: 해당 없음
- 중재 모델: 병렬 할당
- 마스킹: 없음(오픈 라벨)
팔의 수
무기와 개입
참가자 그룹 / 팔참가자 그룹 / 팔 |
개입 / 치료개입 / 치료 |
|---|---|
|
다른: Patients with HSCT-TMA or SOT-TMA
blood and urine collection
|
blood sampling at designated time points
urine collection at designated time points
|
|
다른: Patients after HSCT or SOT with a viral infection, without TMA
blood and urine collection
|
blood sampling at designated time points
urine collection at designated time points
|
|
다른: Patients after HSCT or SOT without a viral infection, without TMA
blood and urine collection
|
blood sampling at designated time points
urine collection at designated time points
|
|
다른: Patients with drug-induced TMA (DITMA)
blood and urine collection
|
blood sampling at designated time points
urine collection at designated time points
|
연구는 무엇을 측정합니까?
주요 결과 측정
주요 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
|
Interferon signature
기간: Time point 1: baseline Time point 2: up to week 52
|
6-gene interferon signature
|
Time point 1: baseline Time point 2: up to week 52
|
|
VEGF-A
기간: Time point 1: baseline Time point 2: up to week 52
|
VEGF-A level
|
Time point 1: baseline Time point 2: up to week 52
|
|
Complement analysis (serum)
기간: Time point 1: baseline Time point 2: up to week 52
|
CH50, AP50, C3, C3d, C4 and C5b-9 at timepoint 1 and C5b-9 at time point 2
|
Time point 1: baseline Time point 2: up to week 52
|
공동 작업자 및 조사자
협력자
협력자
연구 기록 날짜
연구 주요 날짜
연구 시작 (추정된)
연구 시작
기본 완료 (추정된)
기본 완료
연구 완료 (추정된)
연구 완료
연구 등록 날짜
최초 제출
최초 제출
QC 기준을 충족하는 최초 제출
QC 기준을 충족하는 최초 제출
처음 게시됨 (실제)
처음 게시됨
연구 기록 업데이트
마지막 업데이트 게시됨 (실제)
마지막 업데이트 게시됨
QC 기준을 충족하는 마지막 업데이트 제출
QC 기준을 충족하는 마지막 업데이트 제출
마지막으로 확인됨
마지막으로 확인됨
추가 정보
이 연구와 관련된 용어
추가 관련 MeSH 약관
기타 연구 ID 번호
기타 연구 ID 번호
- ROSARIO
개별 참가자 데이터(IPD) 계획
개별 참가자 데이터(IPD)를 공유할 계획입니까?
약물 및 장치 정보, 연구 문서
미국 FDA 규제 의약품 연구
미국 FDA 규제 기기 제품 연구
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