Chronic Eye graft-versus-host disease: what happens after stem cell transplant
Official title: A Multicenter, Prospective, Non-Interventional Observational Cohort Study on Ocular Chronic Graft-Versus-Host Disease After Hematopoietic Stem Cell Transplantation - The Bright Study
Run by Ruijin Hospital · NCT07794800 · Data updated 2026-11-12
This study follows people who had a stem cell transplant to see how many develop chronic ocular graft-versus-host disease and how it affects their daily lives.
Quick facts
| Study type | Observational |
|---|---|
| Ages | 14 Years and up |
| Sex | All |
| Enrollment | 340 (estimated) |
| Sponsor | Ruijin Hospital Academic / other |
| Locations | 1 site (Shanghai, Shanghai Municipality) |
| Status | Recruiting |
| Started | June 1, 2026 |
| Main results expected | June 1, 2030 |
| Study ends | June 1, 2030 |
| Registry record updated | August 31, 2026 |
| Trial ID | NCT07794800 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates are individuals aged 14 years or older who have undergone their first allogeneic stem cell transplant and are at least 100 days post-transplant with confirmed donor engraftment.
✕Probably not a fit
Patients who already have moderate-to-severe ocular surface disease before transplant or who have active ocular infection or other ocular conditions that interfere with assessment may receive limited or no direct benefit from participation.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This is a multicenter, prospective observational study enrolling up to 340 patients who had an allogeneic stem cell transplant. Patients will undergo evaluations by hematology and ophthalmology teams and report outcomes themselves to understand the incidence, risk factors, and clinical course of chronic ocular GVHD after transplant. The study will track patient-reported outcomes and objective eye assessments over time to characterize the condition in routine clinical practice. No experimental treatments are given in this design; it aims to observe natural history and factors associated with outcomes. Results may help clinicians identify patients at higher risk and inform follow-up strategies.
Why it matters
Potential benefit: If successful, the study could improve understanding of chronic ocular GVHD and guide better monitoring and management to preserve vision and quality of life.
How similar studies have gone: Similar observational efforts have provided valuable insights into ocular GVHD patterns, though this study focuses on a structured, multicenter, patient-reported approach in a Chinese population.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Age ≥14 years, both genders eligible; * First allogeneic hematopoietic stem cell transplantation; * 100 days post-transplantation, with donor hematopoietic stem cell engraftment confirmed; * The subject or their legally authorized representative has provided full informed consent, signed the informed consent form, and is willing to complete subsequent follow-up visits Exclusion Criteria: * Preexisting moderate-to-severe ocular surface disease prior to transplantation; * Active ocular infection; * Presence of other ocular conditions that, in the opinion of the ophthalmologist, may significantly affect the diagnosis of chronic ocular graft-versus-host disease, the evaluation of ocular surface parameters, or the completion of long-term follow-up; * Patients with active hematologic malignancies.
Where it's running
-
Ruijin Hospital, Shanghai Jiaotong University School of Medicine
Shanghai, Shanghai Municipality, China Recruiting
Study contacts
- Study coordinator: Chuanhe Jiang
- Email: jch12191@rjh.com.cn
- Phone: 0086-021-64370045
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.