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Efficacy and Safety of Unfractionated Heparin on Severe Sepsis With Suspected Disseminated Intravascular Coagulation - Trial NCT02654561

Access comprehensive clinical trial information for NCT02654561 through Pure Global AI's free database. This Phase 3 trial is sponsored by China Medical University, China and is currently status unknown. The study focuses on Sepsis,Disseminated Intravascular Coagulation. Target enrollment is 700 participants.

This page provides complete trial specifications, intervention details, outcomes, and location information. Pure Global AI offers free access to ClinicalTrials.gov data, helping medical device and pharmaceutical companies navigate clinical research efficiently.

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NCT02654561
Phase 3
drug
Trial Details
ClinicalTrials.gov โ€ข NCT02654561
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Efficacy and Safety of Unfractionated Heparin on Severe Sepsis With Suspected Disseminated Intravascular Coagulation
Phase 3 Study of the Efficacy and Safety of Unfractionated Heparin in Patients With Severe Sepsis/Septic Shock With Suspected DIC

Study Focus

Heparin Sodium

Interventional

drug

Sponsor & Location

China Medical University, China

Haerbin,Changsha,Nanjing,Dalian,Dalian,Shenyang,Shenyang,Qingdao,Chengdu,Kunming,Kunming,Beijing,Beijing,Beijing,Jilin,Qinhuangdao,Shenyang, China

Timeline & Enrollment

Phase 3

Apr 20, 2017

Jun 01, 2021

700 participants

Primary Outcome

ICU mortality

Summary

The primary objective of this study is to estimate the efficacy of unfractionated
 heparin(UFH) on ICU mortality in severe sepsis with suspected DIC.The Second objective is to
 estimate the effect of UFH on 28-day mortality,and the change of the Japanese Association for
 Acute Medicine(JAAM) score and SOFA score. The third one is to evaluate the safety of UFH in
 severe sepsis patients with suspected DIC.

ICD-10 Classifications

Disseminated intravascular coagulation of fetus and newborn
Disseminated intravascular coagulation [defibrination syndrome]
Sepsis, unspecified
Other specified sepsis
Other sepsis

Data Source

ClinicalTrials.gov

NCT02654561

Non-Device Trial