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Construction of Early Diagnosis and Prediction Model for Chronic GVHD Based on Multi target Organ Micro omics

Construction of Early Diagnosis and Prediction Model for Chronic GVHD Based on Multi target Organ Micro omics

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600126762
Enrollment
Unknown
Registered
2026-06-15
Start date
2026-06-30
Completion date
Unknown
Last updated
2026-06-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Skin sclerosis, lichenoid changes

Interventions

The cGVHD case group and the non-CGVHD control group:None

Sponsors

The Second Affiliated Hospital of the Army Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1. Patients aged 18 to 60 years at our center who voluntarily participate in this study and have signed the informed consent form, having undergone allogeneic hematopoietic stem cell transplantation. The diagnostic criteria refer to the Expert Consensus on the Diagnosis and Treatment of Chronic Graft-versus-Host Disease (cGVHD) (2024 Edition). Patients must not have severe impairment of vital systemic organs, as defined by the following criteria: (1) Creatinine = 2 g/dL; (3) Left ventricular ejection fraction > 50%; (4) Hemoglobin > 9 g/dL and bilirubin < 2.0 mg/dL. (5) Complete blood count, liver and kidney function tests, and coagulation profiles must be within normal limits; (6) Pre-transfusion screening tests and hepatitis B five-item serology must all be negative.

Exclusion criteria

Exclusion criteria: 1. Severe complications or high-risk factors: active bleeding disorders (such as coagulation dysfunction, International Normalized Ratio [INR] > 1.5, or platelet count = 3 or expected survival 8.9 mmol/L); hypertension that cannot be reduced to the following range despite treatment with two or fewer antihypertensive agents (systolic blood pressure 2.5 × upper limit of normal (ULN); direct bilirubin (DBIL) and total bilirubin (TBIL) > 2.0 × ULN; serum creatinine > 1.5 × ULN; use of anticoagulant or antiplatelet medications (except low-molecular-weight heparin). 7. Inability to complete the study as required by the investigators.

Design outcomes

Primary

MeasureTime frame
Biomarkers of cGVHD;Performance indicators of the cGVHD diagnostic model;

Countries

China

Contacts

Public ContactWang Xiaoqi

The Second Affiliated Hospital of the Army Medical University

xiaoqiwang27@gmail.com+86 23 68763198

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Jun 29, 2026