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Clinical Trial Details — Status: Withdrawn

Administrative data

NCT number NCT05587881
Other study ID # 2019-nCoVvaccine 01
Secondary ID
Status Withdrawn
Phase
First received
Last updated
Start date January 1, 2022
Est. completion date November 1, 2023

Study information

Verified date January 2022
Source The First Affiliated Hospital of Soochow University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Aim of this study will evaluate the Impact of Covid-19 vaccine on Safety and Efficacy of Hematological Patients Received Allogeneic Hematopoietic Stem Cell Transplantation.


Description:

Since the first detection of a Corona Virus Disease 2019 (COVID-19) infection in late 2019, the syndrome coronavirus-2 (SARS-CoV-2) has spread rapidly across the globe, threatening the health and safety of an increasing number of people. The development of the SARS-CoV-2 vaccine has been shown to be effective in reducing the chance of COVID-19 infection and the severity of the disease. To control the COVID-19 pandemic, an increasing number of studies are calling for people to receive the SARS-CoV-2 vaccine, and the Chinese government is also advocating universal vaccination. However, the investigators have found in our work that as vaccination has become more widespread, clinicians have become somewhat confused about whether they can choose someone who has been vaccinated against SARS-CoV-2 as a donor for a bone marrow transplant, and what is the optimal time for allogeneic hematopoietic stem cell transplantation (allo-HSCT) in vaccined hematological patients. This study will evaluate the impact of Covid-19 vaccine on safety and efficacy of hematological patients received allo-HSCT.


Recruitment information / eligibility

Status Withdrawn
Enrollment 0
Est. completion date November 1, 2023
Est. primary completion date November 1, 2023
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility Inclusion Criteria: 1. Allogeneic hematopoietic stem cell transplantation is expected to start in the short term. 2. Able and willing to provide written informed consent and comply with all requirements for study participation (including all study procedures). Exclusion Criteria: 1. Patients or donors with a history of previous infection with SARS-Cov-2. 2. Patients or donors are currently infected with SARS-Cov-2. 3. Patients have a history of other malignancies, disease progression, or is currently on systemic therapy.

Study Design


Related Conditions & MeSH terms


Intervention

Biological:
COVID-19 vaccine(donor)
Donor received COVID-19 vaccine before stem cells collection.
COVID-19 vaccine(patient)
Patient received COVID-19 vaccine before allo-HSCT.

Locations

Country Name City State
China The First Affiliated Hospital of Soochow University Suzhou Jiangsu

Sponsors (1)

Lead Sponsor Collaborator
The First Affiliated Hospital of Soochow University

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary Disease-free Survival(PFS) To measure the duration of response to allo-HSCT over a follow-up period of 12 months. up to 12 months
Secondary Overall Survival(OS) OS will be assessed from the first day of stem cells infused to death or last follow-up. up to 12 months
Secondary Adverse events profile Number of participants with adverse events. Frequencies of toxicities based on NCI Common Termeinology Criteria for Adverse Events(CTCAE), version 5.0 will be tabulated. Measured 12 months after stem cells infused
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