Overview

rhTPO in Critical Patients With Thrombocytopenia

Status:
Unknown status
Trial end date:
2016-04-01
Target enrollment:
0
Participant gender:
All
Summary
The primary objectives of this study are to assess the impact of rhTPO on mortality among severe sepsis patients with thrombocytopenia, as well as changes of platelet counts and platelet transfusion rates.
Phase:
Phase 2/Phase 3
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Jinling Hospital, China
Criteria
Inclusion Criteria:

- Patients would be include if Diagnosed as sepsis according to ACCP/CCM criteria
Platelet counts is less than 50×109/L for 2 continues days Patient or legally
authorized representative able to provide informed consent

Exclusion Criteria:

- Subject has had a splenectomy for any reason Subject has an active malignancy who is
now under chemotherapy Subject has a known history of bone marrow stem cell disorder
Subject is receiving other investigational agents or procedures Subject is currently
enrolled in, or has completed within the last 30 days, another investigational device
or drug study Subject is pregnant or breast feeding Subject has any kind of disorder
that compromises the ability of the subject to give written informed consent and does
not have a legally acceptable representative Subject has any kind of disorder that
compromises the ability of the subject to comply with study procedures Subject is less
than 18 years or more than 85 years of age History of bone marrow, lung, liver,
pancreas, or small-bowel transplantation Acute pancreatitis with no established source
of infection