🇮🇪Ireland
16°C Partly Cloudy · Dublin
Live Updates
--:--:-- IST
Writer Login
Latest
Clinical Trials in China / NCT06208137
Recruiting Not applicable

Using the Composite Immune Risk Score to Assess and Modulate the Patient's Post-transplant Immune Reconstitution.

NCT06208137 · tracked via the Priya Life Science China tracker
Sponsor
Institute of Hematology & Blood Diseases Hospital, China
Phase
Not applicable
Started
2024-02-29
Last updated
2024-08-13

Condition(s) studied

Transplant-Related Disorder

Investigational drug(s) / intervention(s)

Health monitoring and regular return follow-up reminders

Health monitoring and regular return follow-up reminders: Health monitoring \& reminders for blood tests and follow-up visits until 1 year post-transplant

Study summary

To assess the effectiveness of interventions including health monitoring and regular return follow-up reminders for patients with a high Composite Immune Risk Score.

Eligibility

Sex
ALL
Min age
16 Years
Max age
Healthy volunteers
No
Inclusion Criteria: * 1\) Patients must be ≥ 16 years of age; * 2\) Patients receiving haploidentical allo-HSCT; * 3\) Patients have to sign an informed consent form before the start of the research procedure. Exclusion Criteria: * 1\) Tandem transplantation or multiple transplantations; * 2\) Mental or other medical conditions that make the patients unable to comply with the research treatment and monitoring requirements; * 3\) Patients who are ineligible for the study due to other factors, or will bear great risk if participating in the study.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Institute of Hematology & Blood Diseases Hospital Tianjin Tianjin Municipality Recruiting

More Institute of Hematology & Blood Diseases Hospital, China trials in China

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06208137 on ClinicalTrials.gov ↗ ← All trials in China