Actively Recruiting

Phase 3
Age: 18Years - 80Years
All Genders
NCT05509933

Budesonide Prophylaxis for Engraftment Syndrome After Hematopoietic Cell Transplantation

Led by Henry Ford Health System · Updated on 2026-05-01

110

Participants Needed

1

Research Sites

268 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The purpose of this study is to determine if budesonide prophylaxis starting day 5 after transplant reduces engraftment fever in autologous and allogeneic stem cell transplant recipients.

CONDITIONS

Official Title

Budesonide Prophylaxis for Engraftment Syndrome After Hematopoietic Cell Transplantation

Who Can Participate

Age: 18Years - 80Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients 18 to 80 years old with a diagnosis of a hematological malignancy
  • Meet the bone marrow transplant program criteria to undergo hematopoietic stem cell transplantation for blood cancers
Not Eligible

You will not qualify if you...

  • Patients currently enrolled in other investigational clinical trials
  • Patients undergoing stem cell transplant for non-hematologic malignancies

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

Henry Ford Health System

Detroit, Michigan, United States, 48202

Actively Recruiting

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Research Team

S

shatha farhan

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

PREVENTION

Number of Arms

2

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Budesonide Prophylaxis for Engraftment Syndrome After Hematopoietic Cell Transplantation | DecenTrialz