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RECRUITING
NCT02707497
PHASE2/PHASE3

The Effect of REcombinant Human Thrombopoietin (rhTPO) on Sepsis Patients With aCUte Severe thrombocytopEnia

Sponsor: Ruilan Wang

View on ClinicalTrials.gov

Summary

The purpose of this study is to determine whether recombinant human thrombopoietin(rhTPO) can rapidly increase the platelets counts, shorten the time of the platelet returned to normal, reduce platelet transfusion and bleeding events, prompt recovery of organ function, decrease the length of ICU stay, and eventually reduce the 28-day mortality in sepsis patients with severe thrombocytopenia.

Official title: The Effect of Recombinant Human Thrombopoietin(rhTPO) on Sepsis Patients With Acute Severe Thrombocytopenia:a Prospective, Multi-center, Open-label, ,Randomized, Controlled Trial

Key Details

Gender

All

Age Range

18 Years - 85 Years

Study Type

INTERVENTIONAL

Enrollment

200

Start Date

2019-04-01

Completion Date

2024-09-30

Last Updated

2024-04-18

Healthy Volunteers

No

Interventions

DRUG

rhTPO

Recombinant Human Thrombopoietin,TPIAO®, Shenyang Sunshine Pharmaceutical Company Limited \[SUNSHINE\], Shenyang, China), 15000u/d, qd, subcutaneous injection, daily for no more than 7 consecutive days

DRUG

Placebo

The control group will not use any platelet-increased drugs.

Locations (1)

Shanghai General Hospital, Shanghai Jiaotong University

Shanghai, Shanghai Municipality, China