Allogeneic Hematopoietic Stem Cell Transplantation Cohort Study

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
AgeNot listed
SponsorRuijin Hospital

About this trial

Clinical observational studies using epidemiologic theories and methods. Through the collection of various clinically relevant data, specific outcomes are evaluated in hematologic transplant patients, providing high quality real-world data for clinical practice, informing public health decision-making, and reducing the burden of disease

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

At least one visit to a stem cell transplant center beginning January 1, 2021

Proposed to undergo or have undergone hematopoietic stem cell transplantation

Disqualifiers

Long-term follow-up information for patients not available for any reason (e.g., unavailable or with serious concomitant disease) according to investigator opinion

Due to alcohol and drug addiction thus affecting their ability to follow the requirements of the study

Presence of conditions that could jeopardize patient safety or affect their adherence to the protocol, according to the investigator's opinion

Trial population

Patients who are proposed to undergo or have undergone allogeneic hematopoietic stem cell transplantation

Trial design

Design model

Cohort

Time perspective

Other

Treatments tested in this trial

Not listed

Trial groups

3,000 Participants
are grouped into 1 trial group
Group A: Cohort 1

Trial outcomes

Primary outcomes

1

Overall Survival (OS)

OS since enrollment

Time frame
Time Frame: through study completion, an average of 5 year

Secondary outcomes

1

Strictly complete remission (sCR)

Strictly complete remission (sCR)

Time frame
Time Frame: through study completion, an average of 5 year
2

Complete remission (CR)

Complete remission (CR)

Time frame
Time Frame: through study completion, an average of 5 year
3

Very Good Partial Relief (VGPR)

Very Good Partial Relief (VGPR)

Time frame
Time Frame: through study completion, an average of 5 year
4

Partial remission (PR)

Partial remission (PR)

Time frame
Time Frame: through study completion, an average of 5 year

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.