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Statins and Selective Cyclooxygenase-2 Receptor Inhibitors in Blunt Chest Trauma

Primary Purpose

Blunt Chest Trauma, Acute Respiratory Distress Syndrome

Status
Unknown status
Phase
Not Applicable
Locations
Israel
Study Type
Interventional
Intervention
standard care treatment
Celecoxib
Rosuvastatin
Combined therapy
Sponsored by
Tel-Aviv Sourasky Medical Center
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Blunt Chest Trauma focused on measuring Lung, Contusion, Injury, Cyclooxygenase, Statin

Eligibility Criteria

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

Inclusion Criteria:

  • Patients older than 18 years of age
  • Diagnosis of lung contusion by physical examination, chest xrays, history by the patient, accompanying persons or police.
  • Ability to understand and accept the trial procedures and to sign an informed consent form in accordance with national legislation.
  • Admission to ward

Exclusion Criteria:

  • Penetrating trauma
  • Current use of lipid-lowering therapy, use of non steroidal anti-inflammatory drugs.
  • Current use of postmenopausal hormone-replacement therapy
  • Evidence of hepatic dysfunction (an alanine aminotransferase level more than twice the upper limit of the normal range), a creatine kinase level more than three times the upper limit of the normal range.
  • Creatinine level higher than 2.0 mg/dl
  • Known uncontrolled hypertension (systolic blood pressure >190 mm Hg or diastolic blood pressure >100 mm Hg
  • History of uncontrolled hypothyroidism (thyroid-stimulating hormone level> 1.5 times the upper limit of the normal range)
  • Psychiatric disorders
  • Pregnancy
  • Known allergy or intolerance to one of the protocol drug

Sites / Locations

  • Tel Aviv Sourasky Medical Center

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Other

Active Comparator

Active Comparator

Active Comparator

Arm Label

control

Celecoxib

rosuvastatin

Combined therapy

Arm Description

Group 1: control :(standard care treatment for individual lung contusion inluding analgesia with paracetamol/dypiron/ tramal)

Group 2: Celecoxib 200 mg × 2/d+:(standard care treatment for individual lung contusion inluding analgesia with paracetamol/dypiron/ tramal)

Group 3: Rosuvastatin 40mg × 1/d+:(standard care treatment for individual lung contusion inluding analgesia with paracetamol/dypiron/ tramal)

Group 4: Combined therapy with Celecoxib 200 mg× 2/d + Rosuvastatin 40× 1/d +:(standard care treatment for individual lung contusion inluding analgesia with paracetamol/dypiron/ tramal)

Outcomes

Primary Outcome Measures

1. Signs of ALI, i.e., pneumonia, adult respiratory distress syndrome [ARDS]
1. Signs of ALI, i.e., pneumonia, adult respiratory distress syndrome [ARDS] according to following criteria: Suspected or proven infection Hypoxemia: PaO2/FiO2is ≤300 mm HgBilateral infiltrates consistent with pulmonary edema Positive-pressure mechanical ventilation through an endotracheal tube No clinical evidence of left atrial hypertension to explain bilateral infiltrates Presence of at least three of the four SIRS criteria. If only two criteria are evidenced, one must be temperature or WBC

Secondary Outcome Measures

Full Information

First Posted
June 17, 2012
Last Updated
June 19, 2012
Sponsor
Tel-Aviv Sourasky Medical Center
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1. Study Identification

Unique Protocol Identification Number
NCT01623921
Brief Title
Statins and Selective Cyclooxygenase-2 Receptor Inhibitors in Blunt Chest Trauma
Study Type
Interventional

2. Study Status

Record Verification Date
June 2012
Overall Recruitment Status
Unknown status
Study Start Date
August 2012 (undefined)
Primary Completion Date
August 2013 (Anticipated)
Study Completion Date
August 2013 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Tel-Aviv Sourasky Medical Center

4. Oversight

5. Study Description

Brief Summary
Background: Lung contusion affects 17%-25% of adult blunt trauma patients, and is the leading cause of death from blunt thoracic injury. Statins are lipid-lowering drugs with recently suggested anti-inflammatory and antioxidant properties. Cyclo-oxygenase-2 (COX-2) is a key enzyme in the production of prostaglandins (PG), and evidence suggests that COX-2 plays an important role in the pathogenesis of acute lung injury (ALI). Aims: The current study aims at evaluating the beneficial effects of statins and COX-2 receptor inhibitors on ALI elicited by blunt trauma to the chest. Methods: After approval by the institutional ethics and a scientific committee, and obtaining informed consent , patients admitted to the emergency department (ED) due to blunt trauma with a diagnosis of lung contusion will be enrolled in the study.The effects of statins and COX 2 inhibitors on ALI will be assessed by recording clinical parameters and measuring inflammatory mediators levels in the serum and in the bronchoalveolar space. Expected results: The investigators expect to find that the proposed treatment will be effective in reducing ALI burden. The investigators also suppose that using a combination of those drugs will synergistically potentiate their effect on ALI.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Blunt Chest Trauma, Acute Respiratory Distress Syndrome
Keywords
Lung, Contusion, Injury, Cyclooxygenase, Statin

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
100 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
control
Arm Type
Other
Arm Description
Group 1: control :(standard care treatment for individual lung contusion inluding analgesia with paracetamol/dypiron/ tramal)
Arm Title
Celecoxib
Arm Type
Active Comparator
Arm Description
Group 2: Celecoxib 200 mg × 2/d+:(standard care treatment for individual lung contusion inluding analgesia with paracetamol/dypiron/ tramal)
Arm Title
rosuvastatin
Arm Type
Active Comparator
Arm Description
Group 3: Rosuvastatin 40mg × 1/d+:(standard care treatment for individual lung contusion inluding analgesia with paracetamol/dypiron/ tramal)
Arm Title
Combined therapy
Arm Type
Active Comparator
Arm Description
Group 4: Combined therapy with Celecoxib 200 mg× 2/d + Rosuvastatin 40× 1/d +:(standard care treatment for individual lung contusion inluding analgesia with paracetamol/dypiron/ tramal)
Intervention Type
Drug
Intervention Name(s)
standard care treatment
Intervention Description
Group 1: control :(standard care treatment for individual lung contusion inluding analgesia with paracetamol/dypiron/ tramal)
Intervention Type
Drug
Intervention Name(s)
Celecoxib
Intervention Description
Celecoxib 200 mg × 2/d+:(standard care treatment for individual lung contusion inluding analgesia with paracetamol/dypiron/ tramal)
Intervention Type
Drug
Intervention Name(s)
Rosuvastatin
Intervention Description
Rosuvastatin 40mg × 1/d+:(standard care treatment for individual lung contusion inluding analgesia with paracetamol/dypiron/ tramal)
Intervention Type
Drug
Intervention Name(s)
Combined therapy
Intervention Description
Combined therapy with Celecoxib 200 mg× 2/d + Rosuvastatin 40× 1/d +:(standard care treatment for individual lung contusion inluding analgesia with paracetamol/dypiron/ tramal)
Primary Outcome Measure Information:
Title
1. Signs of ALI, i.e., pneumonia, adult respiratory distress syndrome [ARDS]
Description
1. Signs of ALI, i.e., pneumonia, adult respiratory distress syndrome [ARDS] according to following criteria: Suspected or proven infection Hypoxemia: PaO2/FiO2is ≤300 mm HgBilateral infiltrates consistent with pulmonary edema Positive-pressure mechanical ventilation through an endotracheal tube No clinical evidence of left atrial hypertension to explain bilateral infiltrates Presence of at least three of the four SIRS criteria. If only two criteria are evidenced, one must be temperature or WBC
Time Frame
3 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: Patients older than 18 years of age Diagnosis of lung contusion by physical examination, chest xrays, history by the patient, accompanying persons or police. Ability to understand and accept the trial procedures and to sign an informed consent form in accordance with national legislation. Admission to ward Exclusion Criteria: Penetrating trauma Current use of lipid-lowering therapy, use of non steroidal anti-inflammatory drugs. Current use of postmenopausal hormone-replacement therapy Evidence of hepatic dysfunction (an alanine aminotransferase level more than twice the upper limit of the normal range), a creatine kinase level more than three times the upper limit of the normal range. Creatinine level higher than 2.0 mg/dl Known uncontrolled hypertension (systolic blood pressure >190 mm Hg or diastolic blood pressure >100 mm Hg History of uncontrolled hypothyroidism (thyroid-stimulating hormone level> 1.5 times the upper limit of the normal range) Psychiatric disorders Pregnancy Known allergy or intolerance to one of the protocol drug
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Avi A Weinbroum, MD
Phone
3-6973237
Ext
972
Email
draviw@tasmc.health.gov.il
Facility Information:
Facility Name
Tel Aviv Sourasky Medical Center
City
Tel Aviv
ZIP/Postal Code
64239
Country
Israel
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Avi A Weinbroum, MD
Phone
3-6973237
Ext
972
Email
draviw@tasmc.health.gov.il

12. IPD Sharing Statement

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Statins and Selective Cyclooxygenase-2 Receptor Inhibitors in Blunt Chest Trauma

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