Ulinastatin in Inhalation Lung Injury

NCT01287806 · Status: UNKNOWN · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 120

Last updated 2011-02-01

No results posted yet for this study

Summary

The purpose of this study is to evaluate the efficacy and effect of ulinastatin in inhalation lung injury patients.

Conditions

  • Inhalation Injury

Interventions

DRUG

ulinastatin

Resolved 4 vials of drugs in 100ml physiological saline solution,intravenously infused for 1-2h,tid,for continuous 10days

DRUG

blank group

standard treatment

Sponsors & Collaborators

  • Changhai Hospital

    collaborator OTHER
  • Southwest Hospital, China

    collaborator OTHER
  • General Hospital of Beijing PLA Military Region

    collaborator OTHER
  • Chinese PLA General Hospital

    lead OTHER

Principal Investigators

  • sheng zhiyong, MD · First Hospitals affiliated to the China PLA General Hospital

  • Jia chiyu, MD · First Hospitals affiliated to the China PLA General Hospital

  • Xia zhaofan, MD · Changhai Hospital

  • Pang yizhi, MD · Southwest Hospital, China

  • Chen tunhu, MD · General Hospital of Jinan PLA Military Region

  • Zhu jinmin, MD · General Hospital of Beijing PLA Military Region

  • Liu yi, MD · General Hospital of Lanzhou PLA Military Region

  • Cui xiaolin, MD · Liaonin People's Armed Police Corps Hospital

  • Sheng guanyu, MD · 187 Central Hospital of the Chinese PLA

  • Lu qinjun, MD · 251 Central Hospital of the Chinese PLA

  • Shi shengfu, MD · 322 Central Hospital of the Chinese PLA

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
70 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2011-02-28
Primary Completion
2012-12-31
Completion
2013-01-31

Countries

  • China

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01287806 on ClinicalTrials.gov