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Spatial Transcriptomics and Spatial Proteomics Study of Intestinal Tissue in Patients with Intestinal GVHD and Exploration of Prognostic Biomarkers

Spatial Transcriptomics and Spatial Proteomics Study of Intestinal Tissue in Patients with Intestinal GVHD and Exploration of Prognostic Biomarkers

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500113023
Enrollment
Unknown
Registered
2025-11-24
Start date
2025-12-15
Completion date
Unknown
Last updated
2025-12-01

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

Conditions

Acute graft versus host disease

Interventions

Case group:None
Control group:None

Sponsors

The Second Affiliated Hospital of the Army Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 50 Years

Inclusion criteria

Inclusion criteria: 1. From September 2025 to September 2027, patients aged 18-50 years old who were diagnosed with GI-aGVHD after allogeneic hematopoietic stem cell transplantation were selected as the case group, and patients without GI-aGVHD after allogeneic hematopoietic stem cell transplantation were selected as the control group. 2. Voluntarily participate in this study and sign informed consent; 3. Wthout serious damage of vital organs: (1) creatinine =2g/dl; (3) cardiac ejection index >50%; (4) heme >9g/dL, bilirubin < 2.0mg/dl; 4. Blood routine, liver and kidney function, coagulation routine were normal; 5. There were no other contraindications to intestinal biopsy.

Exclusion criteria

Exclusion criteria: 1.active bleeding caused by drugs or low platelets, and active infection that has not been controlled clinically; 2.Pregnant or lactating women; 3.Severe insufficiency of heart, kidney or liver function; 4.Drug-related or other mucosal diseases and intestinal diseases, diabetes; 5.In cases of clinical symptoms of brain function disorder or severe mental illness, one cannot understand or comply with the research protocol; 6.In cases of clinical symptoms of brain function disorder or severe mental illness, one cannot understand or comply with the research protocol; 7.Researchers believe that other reasons are not suitable for clinical trials;

Design outcomes

Primary

MeasureTime frame
Spatial transcriptomics;

Countries

China

Contacts

Public ContactZhang Xi

The Second Affiliated Hospital of the Army Medical University

zhangxxi@sina.com+86 23 68763198

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026