The Effects of Different Ventilator Strategies on Inflammation and Injury in Normal Lungs

Sponsor
University of Medicine and Dentistry of New Jersey (Other)
Overall Status
Terminated
CT.gov ID
NCT01003730
Collaborator
(none)
1
1
3
12
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Study Details

Study Description

Brief Summary

This research is being done to determine if there is a way the investigators can improve the techniques that they use to assist patients with their breathing during surgery. The majority of surgeries require patients to concurrently undergo general anesthesia. This usually includes a breathing tube and a machine that breathes for the patient during the duration of the surgery. The doctors would like to investigate the effects of this type of anesthesia to healthy adult patients and whether they can improve the way they give general anesthesia to patients. The investigators plan to ask approximately 200 patients to participate. If the patients decide to participate in the study,some additions will be made to the standard anesthetic care they receive. The patients will additionally be monitored for adequate oxygenation in their blood as well as level of inflammation in their blood and lungs. The patients' breathing tube will be bathed with warm normal saline and suctioned twice during the operation. When these procedures are done the patients will be asleep and not be aware of what is happening.

Condition or Disease Intervention/Treatment Phase
  • Other: Ventilator settings
N/A

Detailed Description

The ability to provide mechanical ventilation that will not injure and may protect normal lungs during major surgical procedures of long duration may improve postoperative outcomes and decrease morbidity and mortality. The aim of the current study was to identify ventilator strategies that are less damaging to normal lungs. The investigators plan to compare three ventilation strategies commonly utilized in the operating room in normal lungs. One group will be ventilated with high tidal volume (15 mL/kg PBW) and low PEEP (3 cm H2O), another group ventilated with low tidal volume (6 mL/kg PBW) and low PEEP (3 cm H2O) and the final group ventilated with low tidal volume (6 mL/kg PBW) and high PEEP (10 cm H2O). This study will show the effects of these commonly used methods of ventilation on pulmonary mechanics, systemic and pulmonary inflammatory markers and outcomes in patients with normal lungs undergoing surgery of long duration.

Study Design

Study Type:
Interventional
Actual Enrollment :
1 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Participant)
Primary Purpose:
Treatment
Official Title:
The Effects of Different Ventilator Strategies on Inflammation and Injury in Normal Lungs
Study Start Date :
Mar 1, 2009
Actual Primary Completion Date :
Mar 1, 2010
Actual Study Completion Date :
Mar 1, 2010

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: 1

High tidal volume (15mL/kg PBW0 with low PEEP (3cm H2O

Other: Ventilator settings
Active Comparison of three different parameters of ventilator settings. Results of arterial blood gases and cytokine levels.

Active Comparator: 2

Low tidal volume (6mL/kg PBW) and high PEEP (3cm H2O)

Other: Ventilator settings
Active Comparison of three different parameters of ventilator settings. Results of arterial blood gases and cytokine levels.

Active Comparator: 3

low tidal volume (6mL/kg PBW) and high PEEP (10cm H2O)

Other: Ventilator settings
Active Comparison of three different parameters of ventilator settings. Results of arterial blood gases and cytokine levels.

Outcome Measures

Primary Outcome Measures

  1. cytokine levels in serum and bronchial aspirate [during the operative procedure]

Secondary Outcome Measures

  1. arterial blood gases [during the operative procedure]

  2. subject post-operative outcome:mortality, pulmonary complications, major cardiac morbidity, LOS, readmission [wothin 30 days of surgery]

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 65 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Elective surgery under general anesthesia expected to take 4 hours or more positioned supine for surgery
Exclusion Criteria:
  • Subjects who have HIV or who have had Radiation or chemotherapy for cancer

  • Subjects undergoing surgery on chest or lings

  • Subjects who have obstructive sleep apnea (OSA), asthma, tuberculosis, chronic obstructive pulmonary disease

Contacts and Locations

Locations

Site City State Country Postal Code
1 UMDNJ/University Hospital Newark New Jersey United States 07101

Sponsors and Collaborators

  • University of Medicine and Dentistry of New Jersey

Investigators

  • Principal Investigator: Ellise Delphin, MD, Rutgers, The State University of New Jersey

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
University of Medicine and Dentistry of New Jersey
ClinicalTrials.gov Identifier:
NCT01003730
Other Study ID Numbers:
  • 0120080132
First Posted:
Oct 29, 2009
Last Update Posted:
May 5, 2015
Last Verified:
Apr 1, 2015
Keywords provided by University of Medicine and Dentistry of New Jersey
Additional relevant MeSH terms:

Study Results

No Results Posted as of May 5, 2015