Actively Recruiting
The Safety and Efficacy of Coenzyme I for Injection in Promoting Hematopoietic Recovery of Patients After sUCBT
Led by Anhui Provincial Hospital · Updated on 2024-12-18
12
Participants Needed
1
Research Sites
95 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
To assess the safety and efficacy of coenzyme I for injection in promoting hematopoietic recovery after single-unit unrelated cord blood transplantation in hematological malignancies.
CONDITIONS
Official Title
The Safety and Efficacy of Coenzyme I for Injection in Promoting Hematopoietic Recovery of Patients After sUCBT
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age between 18 and 60 years (inclusive) at screening
- Diagnosed with hematological malignancies to receive single-unit unrelated cord blood transplantation for the first time
- No severe organ failure and no active infections
- ECOG performance status of 0-2
- Voluntarily participating in the clinical trial with full understanding and signed informed consent form
You will not qualify if you...
- Severe organ dysfunction or disease, including heart, liver, kidney, or pancreas
- Pregnant patients
- Refusal by patient or authorized family members to receive Coenzyme I for injection
- Life-threatening disease, physical condition, or organ dysfunction that may risk safety or study results
- Drug dependence, uncontrolled psychiatric disorders, or cognitive impairment
- Participation in other clinical studies affecting hematopoietic recovery within 3 months
- Considered unsuitable by investigator due to anticipated inability to adhere to treatment or examinations
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
The First Affiliated Hospital of University of Science and Technology of China (Anhui Provincial Hospital)
Hefei, Anhui, China, 230036
Actively Recruiting
Research Team
X
Xiaoyu Zhu, Ph.D
CONTACT
Y
Yue Wu, M.D
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SEQUENTIAL
Primary Purpose
TREATMENT
Number of Arms
1
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