Evaluate the Efficacy of Xuebijing Injection in Acute Exacerbations of COPD
Primary Purpose
Pulmonary Disease, Chronic Obstructive
Status
Unknown status
Phase
Phase 4
Locations
China
Study Type
Interventional
Intervention
Xuebijing
Placebo
Sponsored by
About this trial
This is an interventional treatment trial for Pulmonary Disease, Chronic Obstructive focused on measuring Pulmonary Disease, Chronic Obstructive, Xuebijing
Eligibility Criteria
Inclusion Criteria:
- Body weight≥40kg and ≤100kg
- Diagnosis of COPD :(following Global initiative for Chronic Obstructive Lung Disease,GOLD2016)
- Forced Expiratory Volume in 1 second of less than 70% predicted value after bronchodilator
- Acute exacerbation of COPD: the clinical presentation of the patient complaining of an acute change of symptoms(baseline dyspnea,cough,and/or sputum production)that is beyond normal day-to-day variation.
- Assessment of COPD Exacerbations: Medical History:severity of COPD based on degree of airflow limitation;Duration of worsening or new symptoms;Number of previous episodes (total/hospitalizations); Comorbidities; Present treatment regimen;Previous use of mechanical ventilation;
- sign the informed consent
Exclusion Criteria:
- Pregnant women, lactating women;
- Be allergic to Xuebijing;
- Acute exacerbation of COPD onset of more than 72 hours;
- AECOPD with severe hypoxemia:oxygenation index <150 or received Endotracheal intubation invasive mechanical ventilation;
- Participation in another experimental protocol within 30 days of study entry
- Primary diseases:Asthma,Cystic fibrosis,Lung cancer,Tuberculosis,Pulmonary sarcoidosis,Pulmonary interstitial fibrosis,Malignant neoplasms,Blood system diseases,HIV;
- Complications:Pulmonary embolism,shock,DIC,Unstable cardiovascular disease,Upper gastrointestinal bleeding,pneumothorax,Severe liver and kidney dysfunction;
- Mental incompetence or active psychiatric illness
- used the following drugs within 72 hours days of study entry:Ulinastatin,Tanreqing, Reduning,Qingkailing;
- The investigator judged that the subject could not be completed or should not participate in the trial:Hemodialysis more than 1 mouth,Organ transplant patients with potential medical dispute.
Sites / Locations
- Chinese PLA General Hospital
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Placebo Comparator
Arm Label
Xuebijing
Placebo
Arm Description
Xuebijing injection 50ml in 100ml of Normal Saline IV, in 80mins, per 12 hours. administration of the agent for consecutive 5 days
Normal Saline 150ml IV, in 80mins, per 12 hours. administration of the agent for consecutive 5 days
Outcomes
Primary Outcome Measures
Invasive mechanical ventilation rate
Invasive mechanical ventilation rate in %
Secondary Outcome Measures
length of Hospital stay
Invasive mechanical ventilation rate in days
Full Information
NCT ID
NCT02937974
First Posted
October 13, 2016
Last Updated
October 18, 2016
Sponsor
Chinese PLA General Hospital
Collaborators
First Hospitals affiliated to the China PLA General Hospital, Navy General Hospital, Beijing, Rocket Force General Hospital,Chinese People's Liberation Army, 307 Hospital of PLA, Beijing Shijitan Hospital, Capital Medical University
1. Study Identification
Unique Protocol Identification Number
NCT02937974
Brief Title
Evaluate the Efficacy of Xuebijing Injection in Acute Exacerbations of COPD
Official Title
Evaluate the Efficacy of Xuebijing Injection in Acute Exacerbations of COPD:a Multicentre Randomised Controlled Trial
Study Type
Interventional
2. Study Status
Record Verification Date
October 2016
Overall Recruitment Status
Unknown status
Study Start Date
October 2016 (undefined)
Primary Completion Date
December 2018 (Anticipated)
Study Completion Date
December 2018 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Chinese PLA General Hospital
Collaborators
First Hospitals affiliated to the China PLA General Hospital, Navy General Hospital, Beijing, Rocket Force General Hospital,Chinese People's Liberation Army, 307 Hospital of PLA, Beijing Shijitan Hospital, Capital Medical University
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Objective: A prospective multicenter randomized controlled trial to assess the efficacy and safety of Xuebijing injection for acute exacerbation of chronic obstructive pulmonary disease(AECOPD).
Methods: 254 AECOPD inpatients will be recruited in 6 hospitals in China over 2 years. They will be randomly assigned to Experimental group and Placebo group,Experimental: Xuebijing injection 50ml in 100ml of Normal Saline IV, in 80mins, per 12 hours. administration of the agent for consecutive 5 days;Placebo Comparator: Normal Saline 150ml IV, in 80mins, per 12 hours. administration of the agent for consecutive 5 days. Compare the following index between the two groups: Invasive mechanical ventilation rate, length of hospital stay, Treg cell,Th1,Th2,HLA-DR,CRP,PCT,IL-4,IL-6,IL-10,TNF-α,IFN-γ, APACHEⅡ, CAPS score.
Detailed Description
A prospective multicenter randomized controlled trial to assess the efficacy and safety of Xuebijing injection for acute exacerbation of chronic obstructive pulmonary disease(AECOPD).
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Pulmonary Disease, Chronic Obstructive
Keywords
Pulmonary Disease, Chronic Obstructive, Xuebijing
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
254 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Xuebijing
Arm Type
Experimental
Arm Description
Xuebijing injection 50ml in 100ml of Normal Saline IV, in 80mins, per 12 hours. administration of the agent for consecutive 5 days
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Normal Saline 150ml IV, in 80mins, per 12 hours. administration of the agent for consecutive 5 days
Intervention Type
Drug
Intervention Name(s)
Xuebijing
Intervention Description
Xuebijing injection 50ml in 100ml of Normal Saline IV, in 80mins, per 12 hours. administration of the agent for consecutive 5 days
Intervention Type
Drug
Intervention Name(s)
Placebo
Intervention Description
Normal Saline 150ml IV, in 80mins, per 12 hours. administration of the agent for consecutive 5 days
Primary Outcome Measure Information:
Title
Invasive mechanical ventilation rate
Description
Invasive mechanical ventilation rate in %
Time Frame
28 days
Secondary Outcome Measure Information:
Title
length of Hospital stay
Description
Invasive mechanical ventilation rate in days
Time Frame
28 days
10. Eligibility
Sex
All
Minimum Age & Unit of Time
40 Years
Maximum Age & Unit of Time
85 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Body weight≥40kg and ≤100kg
Diagnosis of COPD :(following Global initiative for Chronic Obstructive Lung Disease,GOLD2016)
Forced Expiratory Volume in 1 second of less than 70% predicted value after bronchodilator
Acute exacerbation of COPD: the clinical presentation of the patient complaining of an acute change of symptoms(baseline dyspnea,cough,and/or sputum production)that is beyond normal day-to-day variation.
Assessment of COPD Exacerbations: Medical History:severity of COPD based on degree of airflow limitation;Duration of worsening or new symptoms;Number of previous episodes (total/hospitalizations); Comorbidities; Present treatment regimen;Previous use of mechanical ventilation;
sign the informed consent
Exclusion Criteria:
Pregnant women, lactating women;
Be allergic to Xuebijing;
Acute exacerbation of COPD onset of more than 72 hours;
AECOPD with severe hypoxemia:oxygenation index <150 or received Endotracheal intubation invasive mechanical ventilation;
Participation in another experimental protocol within 30 days of study entry
Primary diseases:Asthma,Cystic fibrosis,Lung cancer,Tuberculosis,Pulmonary sarcoidosis,Pulmonary interstitial fibrosis,Malignant neoplasms,Blood system diseases,HIV;
Complications:Pulmonary embolism,shock,DIC,Unstable cardiovascular disease,Upper gastrointestinal bleeding,pneumothorax,Severe liver and kidney dysfunction;
Mental incompetence or active psychiatric illness
used the following drugs within 72 hours days of study entry:Ulinastatin,Tanreqing, Reduning,Qingkailing;
The investigator judged that the subject could not be completed or should not participate in the trial:Hemodialysis more than 1 mouth,Organ transplant patients with potential medical dispute.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Lixin Xie, Professor
Organizational Affiliation
Chinese PLA General Hospital
Official's Role
Study Director
Facility Information:
Facility Name
Chinese PLA General Hospital
City
Beijing
ZIP/Postal Code
100853
Country
China
12. IPD Sharing Statement
Plan to Share IPD
Undecided
Citations:
PubMed Identifier
19729666
Citation
Freeman CM, Martinez FJ, Han MK, Ames TM, Chensue SW, Todt JC, Arenberg DA, Meldrum CA, Getty C, McCloskey L, Curtis JL. Lung dendritic cell expression of maturation molecules increases with worsening chronic obstructive pulmonary disease. Am J Respir Crit Care Med. 2009 Dec 15;180(12):1179-88. doi: 10.1164/rccm.200904-0552OC. Epub 2009 Sep 3.
Results Reference
background
PubMed Identifier
30777117
Citation
Xie S, Yan P, Yao C, Yan X, Huo Y, Zhang J, Liu S, Feng Z, Shang H, Xie L. Efficacy and safety of Xuebijing injection and its influence on immunomodulation in acute exacerbations of chronic obstructive pulmonary disease: study protocol for a randomized controlled trial. Trials. 2019 Feb 18;20(1):136. doi: 10.1186/s13063-019-3204-z.
Results Reference
derived
Links:
URL
https://www.ncbi.nlm.nih.gov/pubmed/?term=19729666
Description
19729666
Learn more about this trial
Evaluate the Efficacy of Xuebijing Injection in Acute Exacerbations of COPD
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