Skip to main content
OpenTrials
Completed

NCT Number: NCT03475732

Pharmacokinetics of XueBiJing in Patients With Sepsis

Pharmacokinetics and disposition of XueBiJing compounds in patients with sepsis

Completed

Looking for future studies?

Notify Me

Key information

Age range

18 year–70 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Zhongda Hospital, Southeast University

Nanjing, Jiangsu, 210009, China

About this study

XueBiJing injection, a five-herb combination approved by Chinese FDA in 2004, has been widely used as an add-on therapy in routine sepsis care in Chinese clinics. A comprehensive pharmacokinetic research on this herbal injection has been conducted in healthy human subjects, and the major circulating XueBiJing compounds, as well as their systemic exposure levels and forms and pharmacokinetic characteristics, have been identified. However, it is known that sepsis may induce hepatic, renal and cardiac dysfunction, alter drug metabolizing enzymes and transporters activities, increase capillary permeability, and induce various pathophysiological changes. All these will affect the concentrations at the action sites and pharmacokinetic characteristics of XueBiJing compounds, which contribute to the injection's overall therapeutic action, thus influencing the anti-septic efficacy of the injection. The purpose of this prospective, open label study is to identify the circulating XueBiJing compounds in patients with sepsis after intravenously dosing XueBiJing injection and their systemic exposure forms and levels, pharmacokinetic characteristics, and the associated inter-patient differences of these XueBiJing compounds.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • 18≤ age ≤70 years old
  • Community acquired pneumonia patients who met the Sepsis-3 criteria from Society of Critical Care Medicine (SCCM) /European Society of Intensive Care Medicine (ESICM) with2 ≤SOFA ≤13
  • To use XueBiJing injection as an add-on therapy to treat sepsis decided byclinician
  • Informed consent obtained

Exclusion criteria

  • Diagnosis of sepsis for over 48 h
  • Pregnant or lactating women
  • Patients with a history of anaphylaxis or allergyto XueBiJing or its component herbs
  • Patients participated in an investigational clinical trial within 30 days prior to this study
  • Patients unable or unsuitable to participate in this study decided by the investigator (i.e., patients whose death are deemed within 48 h or who poorly adhere to the treatment)

Treatment and study plan

Xuebijing Injection

Drug

100mL XueBiJing injection (dissolved with 100 mL of 0.9% normal saline),intravenous infusion for 1.25 h, q12h for 5 days

Other names: Tianjin Chase Sun Pharmaceutical Co. LTD

Primary outcomes

  1. Plasma concentrations of XueBiJing injection compounds

    Time frame: On 1stand 5th day of giving XueBiJing injection: pre-dose, 1.25 h after starting the infusion, and 0.5, 1, 2, 4, and 8 h after terminating the infusion On 2nd to 4th day of giving XueBiJing injection: pre-dose and 1.25 h after starting the infusion

    Plasma concentrations of XueBiJing injection compounds

Secondary outcomes

  1. Accumulative amounts of XueBiJing compounds in urine

    Time frame: On 1st day of giving XueBiJing injection: pre-dose and 0-3.25 and 3.25-12 h after starting the infusion On 5thday of giving XueBiJing injection:0-3.25 and 3.25-12 h after starting the infusion

    Accumulative amounts of XueBiJing compounds in urine

Sponsors and collaborators

Lead sponsor

Southeast University, China

Other

Collaborators

  • Chinese Academy of Sciences

Registry information

Official study title

Pharmacokinetic Study of XueBiJing Injection in Patients With Sepsis

Important dates

Study start
2018
Primary completion
2019
Study completion
2019
First posted
Mar 23, 2018
Registry last updated
Jan 5, 2021

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.