Actively Recruiting

All Genders
NCT06441669

Effect of Letermovir Prophylaxis on CMV-specific Immune Reconstitution Post UCBT

Led by Anhui Provincial Hospital · Updated on 2024-06-04

60

Participants Needed

1

Research Sites

107 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

To explore the effect of letermovir prophylaxis on cytomegalovirus-specific immune reconstitution post unrelated cord blood transplantation

CONDITIONS

Official Title

Effect of Letermovir Prophylaxis on CMV-specific Immune Reconstitution Post UCBT

Who Can Participate

All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients are receiving a first unrelated cord blood transplantation (UCBT).
  • Patients start letermovir prophylaxis within 0-28 days post UCBT.
Not Eligible

You will not qualify if you...

  • Patients having active CMV DNAemia at the time of letermovir initiation.
  • Patients recruited in a clinical study on an anti-CMV trial.

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Anhui Provincial Hospital

Hefei, Anhui, China

Actively Recruiting

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Research Team

X

Xiaoyu Zhu, ph.D

CONTACT

B

Bingbing Yan

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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Effect of Letermovir Prophylaxis on CMV-specific Immune Reconstitution Post UCBT | DecenTrialz