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The Effect of Ulinastatin on Bronchoalveolar Lavage Fluid of Inflammatory Factors in Patients With Ventilator-associated Pneumonia

Primary Purpose

Ventilator-associated Bacterial Pneumonia, Mechanical Ventilation Complication

Status
Unknown status
Phase
Phase 2
Locations
China
Study Type
Interventional
Intervention
Ulinaststin for injection
placebo
Sponsored by
Shanghai Minhang Central Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Ventilator-associated Bacterial Pneumonia focused on measuring ventilator-associated pneumonia, mechanical ventilation, ulinastatin for injection, bronchoalveolar lavage fluid, inflammatory factors

Eligibility Criteria

18 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • All consecutive patients with ventilator-associated pneumonia(VAP) who are admitted to the intensive care unit between 1st January 2014 at 0:00(midnight) and the finish date of 31st December 2015 at 23:59 (11:59 pm).
  • Informed consent.

Exclusion Criteria:

  • Patients with pneumonia when they are admitted to ICU.
  • Ulinastatin was previous used before the patients were diagnosed VAP.
  • Active gastropathic disorder.
  • Be allergic to ulinastatin.
  • Pregnancy.
  • Unwilling to continue the therapy during hospitalization.

Sites / Locations

  • Shanghai Minhang Central Hospital

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Experimental

Placebo Comparator

Arm Label

NUTIG

HUTIG

CG

Arm Description

The normal dose of ulinastatin for injection group(NUTIG): Ulinastatin(Techpool inc,Guangdong,China) was administered to the group as a bolus of 100,000 U diluted in 100 mL of normal saline every 8 hour.A course of treatment consisted of 7 days after the patients were diagnosed as VAP.

The high dose of ulinastatin for injection group(HUTIG): Ulinastatin(Techpool inc,Guangdong,China) was administered to the group as a bolus of 200,000 U diluted in 100 mL of normal saline every 8 hour.A course of treatment consisted of 7 days after the patients were diagnosed as VAP.

The compare group(CG): The group was given 100 mL of normal saline every 8 hour.A course of treatment consisted of 7 days after the patients were diagnosed as VAP.

Outcomes

Primary Outcome Measures

Levels of inflammatory factors in bronchoalveolar lavage fluid and blood serum.
The variety of tumor necrosis factor-α(TNF-α),interleukin-10(IL-10),interleukin-18(IL-18) and interferon-γ(INF-γ) in bronchoalveolar lavage fluid and blood serum are observed.

Secondary Outcome Measures

All cause mortality.
Ventilation free days.
Antibiotic free days.
Percentage of MDR pathogenic bacteria.
We will find whether the bacteria of multidrug-resistance can be isolated from the bronchoalveolar lavage fluid culture. We will count the number of methicillin-resistant staphylococcus aureus(MRSA),extended-spectrum beta-lactamase(ESBLs) or vancomycin-resistant enterococcus(VRE) isolated from bronchoalveolar lavage fluid culture.
Oxygenation index
Oxygenation index = Fio2/PaO2(mmHg)

Full Information

First Posted
May 24, 2013
Last Updated
May 29, 2013
Sponsor
Shanghai Minhang Central Hospital
Collaborators
Ruijin Hospital, RenJi Hospital, Shanghai Jiao Tong University School of Medicine
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1. Study Identification

Unique Protocol Identification Number
NCT01865266
Brief Title
The Effect of Ulinastatin on Bronchoalveolar Lavage Fluid of Inflammatory Factors in Patients With Ventilator-associated Pneumonia
Official Title
The Effect of Ulinastatin on Bronchoalveolar Lavage Fluid of Inflammatory Factors in Patients With Ventilator-associated Pneumonia
Study Type
Interventional

2. Study Status

Record Verification Date
May 2013
Overall Recruitment Status
Unknown status
Study Start Date
January 2014 (undefined)
Primary Completion Date
December 2015 (Anticipated)
Study Completion Date
June 2016 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Shanghai Minhang Central Hospital
Collaborators
Ruijin Hospital, RenJi Hospital, Shanghai Jiao Tong University School of Medicine

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Ventilator-associated pneumonia (VAP) is an important cause of morbidity and mortality in ventilated critically ill patients specially in intensive care unit (ICU). It is associated with an increased duration of mechanical ventilation, high death rates and increased healthcare costs in the development country. Although VAP is preventable and many practices have been demonstrated to reduce the incidence of this disease, the morbidity is still so high. VAP is hard to cure and the mortality is about to 40% which was reported in China in 2004. If the bacteria of multidrug-resistance(MDR) is isolated, the mortality can increase to 70%. So much more methods should be needed in treating VAP in addition to using antibiotics. Ulinastatin is a serine protease inhibitor with a molecular weight of 67,000 found in healthy human urine. It is used worldwide for patients with inflammatory disorders, including disseminated intravascular coagulation(DIC),shock, and pancreatitis . Furthermore, ulinastatin administration can help reduce sepsis, prevent multiple organ dysfunction, and modulate immune functions. Actually, three studies have showed that ulinastatin treatment is associated with reduced the levels of inflammatory factors in blood serum in patients with acute respiratory distress syndrome(ARDS).Though analyses of serum inflammatory factors such as tumor necrosis factor (TNF)-α and interleukin (IL)-6 have been used to determine the degree of systemic inflammation under various clinical conditions, they can not reflect the degrees of lung infection directly. Basing on the results of previous studies, meta analyses and system reviews, the investigators hypothesized that the anti-inflammatory function of ulinaststin may also decrease the levels of inflammatory factors in bronchoalveolar lavage(BAL) fluid in Patients with VAP. In addition there is no prospective study to investigate the role of ulinastatin in BAL. The investigator hopes that this study can approve the relationship between ulinastatin and inflammatory factors in BAL. And it can improve the processes,outcomes and costs of critical care as well.
Detailed Description
This is a one-center, three-arm, randomized, single-blinded, controlled trial. When a patient was diagnosed VAP during mechanic ventilation in ICU,a sealed envelop will be opened which decide whether the patient is assigned to the normal dose ulinastatin group,the high dose ulinastatin group or the compare group. VAP diagnosis and treatment accord with the "Comprehensive evidence-based clinical practice guidelines for ventilator-associated pneumonia:Diagnosis and treatment" which was published in 2008 by Canadian critical care trials group. The aim of the present study is to determine the efficacy of ulinastatin for the treatment of ventilator-associated Pneumonia(VAP) and to investigate the effect to inflammatory factors in bronchoalveolar lavage fluid .

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Ventilator-associated Bacterial Pneumonia, Mechanical Ventilation Complication
Keywords
ventilator-associated pneumonia, mechanical ventilation, ulinastatin for injection, bronchoalveolar lavage fluid, inflammatory factors

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2, Phase 3
Interventional Study Model
Parallel Assignment
Masking
Participant
Allocation
Randomized
Enrollment
60 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
NUTIG
Arm Type
Experimental
Arm Description
The normal dose of ulinastatin for injection group(NUTIG): Ulinastatin(Techpool inc,Guangdong,China) was administered to the group as a bolus of 100,000 U diluted in 100 mL of normal saline every 8 hour.A course of treatment consisted of 7 days after the patients were diagnosed as VAP.
Arm Title
HUTIG
Arm Type
Experimental
Arm Description
The high dose of ulinastatin for injection group(HUTIG): Ulinastatin(Techpool inc,Guangdong,China) was administered to the group as a bolus of 200,000 U diluted in 100 mL of normal saline every 8 hour.A course of treatment consisted of 7 days after the patients were diagnosed as VAP.
Arm Title
CG
Arm Type
Placebo Comparator
Arm Description
The compare group(CG): The group was given 100 mL of normal saline every 8 hour.A course of treatment consisted of 7 days after the patients were diagnosed as VAP.
Intervention Type
Drug
Intervention Name(s)
Ulinaststin for injection
Intervention Type
Drug
Intervention Name(s)
placebo
Primary Outcome Measure Information:
Title
Levels of inflammatory factors in bronchoalveolar lavage fluid and blood serum.
Description
The variety of tumor necrosis factor-α(TNF-α),interleukin-10(IL-10),interleukin-18(IL-18) and interferon-γ(INF-γ) in bronchoalveolar lavage fluid and blood serum are observed.
Time Frame
7 days
Secondary Outcome Measure Information:
Title
All cause mortality.
Time Frame
30 days
Title
Ventilation free days.
Time Frame
30 days
Title
Antibiotic free days.
Time Frame
30 days
Title
Percentage of MDR pathogenic bacteria.
Description
We will find whether the bacteria of multidrug-resistance can be isolated from the bronchoalveolar lavage fluid culture. We will count the number of methicillin-resistant staphylococcus aureus(MRSA),extended-spectrum beta-lactamase(ESBLs) or vancomycin-resistant enterococcus(VRE) isolated from bronchoalveolar lavage fluid culture.
Time Frame
30 days
Title
Oxygenation index
Description
Oxygenation index = Fio2/PaO2(mmHg)
Time Frame
30 days
Other Pre-specified Outcome Measures:
Title
Adverse effects
Description
The adverse effects from using ulinastatin. Irritability,nausea,vomit,diarrhoea or the aspartate transaminaseere and alanine transaminase are more than one time the upper normal limit were regarded as the adverse effects.
Time Frame
30 days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: All consecutive patients with ventilator-associated pneumonia(VAP) who are admitted to the intensive care unit between 1st January 2014 at 0:00(midnight) and the finish date of 31st December 2015 at 23:59 (11:59 pm). Informed consent. Exclusion Criteria: Patients with pneumonia when they are admitted to ICU. Ulinastatin was previous used before the patients were diagnosed VAP. Active gastropathic disorder. Be allergic to ulinastatin. Pregnancy. Unwilling to continue the therapy during hospitalization.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Yu YueTian, MD
Phone
13818227011
Email
fishyyt@sina.com
First Name & Middle Initial & Last Name or Official Title & Degree
Liu ChunYan, MD
Phone
13917836226
Email
doctorlcy@sina.com
Facility Information:
Facility Name
Shanghai Minhang Central Hospital
City
Shanghai
ZIP/Postal Code
201199
Country
China
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Yu YueTian, MD
Phone
13818227011
Email
fishyyt@sina.com
First Name & Middle Initial & Last Name & Degree
Liu ChunYan, MD
Phone
13917836226
Email
doctorlcy@sina.com
First Name & Middle Initial & Last Name & Degree
Yu YueTian, MD
First Name & Middle Initial & Last Name & Degree
Mao EnQiang, MD

12. IPD Sharing Statement

Learn more about this trial

The Effect of Ulinastatin on Bronchoalveolar Lavage Fluid of Inflammatory Factors in Patients With Ventilator-associated Pneumonia

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