We are updating the design of this site. Learn more.
Show more
ClinicalTrials.gov Menu

Protective Variable Ventilation for Open Abdominal Surgery (PROVAR)

This study has been completed.
ClinicalTrials.gov Identifier:
First Posted: September 12, 2012
Last Update Posted: March 31, 2016
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by (Responsible Party):
Technische Universität Dresden
Variable ventilation has been shown to improve lung function and reduce lung damage as well as inflammation in different models of the acute respiratory distress syndrome. Also, variable ventilation is able to recruit lungs. The present study will investigate whether variable as compared to non-variable ventilation improves post-operative lung function and reduces systemic inflammation in patients submitted to open abdominal surgery.

Condition Intervention
Development of Pulmonary Dysfunction Following Open Abdominal Surgery Other: Variable Ventilation

Study Type: Interventional
Study Design: Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Triple (Participant, Investigator, Outcomes Assessor)
Primary Purpose: Treatment
Official Title: Effects of Variable Tidal Volumes During Open Abdominal Surgery on Lung Function and Systemic Inflammation

Further study details as provided by Technische Universität Dresden:

Primary Outcome Measures:
  • Forced vital capacity [ Time Frame: Preoperative until 5th postoperative day ]
    Forced vital capacity is assessed on the first postoperative day

Secondary Outcome Measures:
  • Arterial partial CO2 pressure [ Time Frame: Preoperative until 5th postoperative day ]
    PacO2 on the first postoperative day

  • Peak expiratory flow [ Time Frame: Preoperative until 5th postoperative day ]
  • Forced expiratory volume after 1 sec [ Time Frame: Preoperative until 5th postoperative day ]
    Forced expiratory volume after 1 sec (FEV1) on first postoperative day

  • PaO2/FIO2 [ Time Frame: Preoperative until 5th postoperative day ]
    PaO2/FIO2 during the intraoperative period

  • Distribution of ventilation [ Time Frame: Preoperative until 5th postoperative day ]
    Distribution of ventilation in lungs

  • Atelectasis [ Time Frame: Preoperative until 5th postoperative day ]
    Amount of lung atelectasis on the first postoperative day

  • Postoperative pulmonary complications [ Time Frame: Preoperative until discharge from hospital ]
    Development of postoperative pulmonary complications

  • Inflammation markers [ Time Frame: Preoperative until 5th postoperative day ]
    Concentrations of interleukine(IL)-6, IL-8 and tumor necrosis factor(TNF)-alpha in plasma

Enrollment: 50
Study Start Date: September 2012
Study Completion Date: September 2013
Primary Completion Date: September 2013 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Active Comparator: Variable Ventilation
Variable tidal volumes with mean at 8 mL/kg of predicted body weight
Other: Variable Ventilation
No Intervention: Non-variable Ventilation
Conventional mechanical ventilation with tidal volume 8 mL/kg of predicted body weight


Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.

Ages Eligible for Study:   18 Years to 85 Years   (Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No

Inclusion Criteria:

  • elective open abdominal surgery
  • ASA classification 2-3
  • age between 18 und 85 yrs
  • expected duration of surgery > 3 h
  • expected extubation in the operation room
  • written informed consent

Exclusion Criteria:

  • chronic lung disease (except to COPD stadium I and II, and asthma)
  • Body Mass Index (BMI) > 40
  • allergy to one of the drugs to be used for general anesthesia
  • participation in another interventional trial within 4 weeks before enrollment
  • addiction or any other disease that may interfere with the capacity of giving informed consent
  • pregnant or breastfeeding women
  • women in reproductive age, except to those who fulfill one of the following:

    • post-menopause (12 months natural amenorrhoea, or 6 months amenorrhoea and serum FSH > 40 mlU/ml
    • post-operative (6 weeks after two-sided ovariectomy)
    • routine and correct use of anticonceptional methods with failure rate < 1 % per year
    • sexually not active
    • vasectomy of the partner
  • indication of low compliance with the protocol
  • contraindication for MRI examination
  Contacts and Locations
Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01683578

Department of Anesthesiology and Intensive Care, University Hospital Carl Gustav Carus
Dresden, Saxony, Germany, 01307
Sponsors and Collaborators
Technische Universität Dresden
Principal Investigator: Marcelo Gama de Abreu, MD, PhD Klinikum Ludwigshafen
  More Information

Additional Information:
Publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
Responsible Party: Technische Universität Dresden
ClinicalTrials.gov Identifier: NCT01683578     History of Changes
Other Study ID Numbers: PulmEngineering-2012-01
First Submitted: September 3, 2012
First Posted: September 12, 2012
Last Update Posted: March 31, 2016
Last Verified: March 2016

Keywords provided by Technische Universität Dresden:
mechanical ventilation
lung function
abdominal surgery, open
systemic inflammation