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Is Peri-operative Hyperoxemia a Risk Factor for Postoperative Complications? (HYPEROXIA)

Primary Purpose

Vascular Disease

Status
Completed
Phase
Phase 3
Locations
Sweden
Study Type
Interventional
Intervention
Oxygen
Air
Sponsored by
Örebro University, Sweden
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Vascular Disease focused on measuring postoperative complications, postoperative cognitive dysfunction, oxygen

Eligibility Criteria

65 Years - undefined (Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Patients undergoing elective vascular surgery (peripheral or aortic surgery),
  • No language or cognitive disability
  • Written, informed consent

Exclusion Criteria:

  • Patients with COPD/other lung diseases that require preoperative oxygen therapy
  • Patients undergoing carotid artery surgery

Sites / Locations

  • University Hospital
  • Örebro University Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

Supplemental Oxygen

Air or supplemental oxygen

Arm Description

Inspired oxygen fraction > 0.5 and SpO2 = 98-100%

Air or lowest possible inspired concentration of oxygen to maintain SpO2 > 90%

Outcomes

Primary Outcome Measures

Composite morbidity
Major complications such as MACE, TIA/stroke/renal insufficiency/POCD etc

Secondary Outcome Measures

Long term outcome (Major complications)
Major complications
Specific outcomes (Major adverse cardiac events (MACE))
Major adverse cardiac events (MACE)
Specific outcomes (TIA or stroke)
TIA or stroke
Specific outcomes (renal insufficiency including dialysis or renal failure)
renal insufficiency including dialysis or renal failure

Full Information

First Posted
November 15, 2014
Last Updated
March 2, 2021
Sponsor
Örebro University, Sweden
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1. Study Identification

Unique Protocol Identification Number
NCT02562781
Brief Title
Is Peri-operative Hyperoxemia a Risk Factor for Postoperative Complications?
Acronym
HYPEROXIA
Official Title
Is Peri-operative Hyperoxemia a Risk Factor for Postoperative Complications? A Randomised, Prospective Study in Patients Undergoing Vascular Surgery
Study Type
Interventional

2. Study Status

Record Verification Date
March 2021
Overall Recruitment Status
Completed
Study Start Date
November 2014 (undefined)
Primary Completion Date
December 2020 (Actual)
Study Completion Date
January 2021 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Örebro University, Sweden

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Patients undergoing vascular surgery are at a significantly high risk of perioperative cardiovascular, cerebral and renal events compared to those undergoing non-vascular surgery. This could be because of co-morbidities that are common in this patient group. Additionally, smoking, which is common in this population, may be a contributing factor. Oxygen therapy has been used for decades in order to reduce the risk of myocardial infarction and stroke in patients undergoing vascular surgery and pre-existing co-morbidities in the belief that increased inspired oxygen increases oxygen delivery to tissues, thereby reducing the risk for hypoxia and cell death. However, several studies published recently have questioned the routine use of high inspired oxygen concentration (hyperoxia) to improve oxygen delivery, specifically in the neonatal period but possibly even following myocardial infarction. This could be explained by the fact that increasing inspired concentrations of oxygen cause vasoconstriction in cerebral and coronary arteries, thereby reducing blood flow. Additionally, increased oxygen causes excessive production of reactive oxygen species (ROS), and repercussion injury from oxidative stress. The latter can lead to apoptosis (cell death) in myocardial or cerebral neurons. Despite the high risks of administering oxygen when not needed, it is routinely used in hospitals all over the world without a doctors prescription. This study aims to assess peri-operative complications up to 1 year following vascular surgery in patients randomised to receive high inspired oxygen concentration (endpoint: SpO2 98 - 100%) or minimal inspired O2 concentration (endpoint: SpO2 > 90%).
Detailed Description
Oxygen is probably one of the commonest "non-prescription" drug used in the hospital and its advantage in several situations including carbon monoxide poisoning, central hypoxia and prior to planned intubation in an acute situation are today well-established and commonly used. Oxygen has been frowned upon in the resuscitation of newborn babies because of the risk of retrolental hypoplasia, now well accepted and adopted in clinical practice. Oxygen has also been traditionally used to increase oxygen carrying capacity in patients presenting with an acute coronary syndrome (ACS), to reduce surgical site infections (SSI), to ensure adequate oxygen delivery to tissues in unconscious patients, during cardiac surgery and for postoperative management, specifically after major surgery. Thus, deliberate use of high inspiratory oxygen concentrations (e.g., 80% or above) is recommended in the treatment of specific intoxications, such as with carbon monoxide or cyanide, wherein hyperbaric oxygen should also be considered. In addition, a high oxygen fraction has been suggested to prevent adverse outcomes after surgery and anesthesia, including a reduction in wound infections and postoperative nausea and vomiting (PONV). In critically ill patients, oxygen delivery to the tissues is often compromised, and supplemental oxygen (e.g., face mask with 10 L oxygen per min) is commonly administered to patients with pneumonia, sepsis, acute coronary syndrome, or stroke - in fact, it is estimated that oxygen is given during transport in approximately one-third of all ambulance journeys. Several reports published recently have questioned many of the "routine" uses of oxygen and some evidence even seems to point towards negative outcomes in some of these conditions. Specifically, excessive oxygen is likely to do more harm than good in the neonatal period, following cardio-pulmonary resuscitation and likely following acute myocardial infarction. Prospective, randomised studies on this important use of oxygen in the preoperative string are, however, lacking in the literature and in view of theoretical risks for hyperoxemia to several organs, the routine use of high oxygen fractions during the peri-operative phase can be questioned. This study aims to assess peri-operative complications up to 1 year following vascular surgery in patients randomised to receive high inspired oxygen concentration (endpoint: SpO2 98 - 100%) or minimal inspired O2 concentration (endpoint: SpO2 > 90%).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Vascular Disease
Keywords
postoperative complications, postoperative cognitive dysfunction, oxygen

7. Study Design

Primary Purpose
Other
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
Participant
Allocation
Randomized
Enrollment
184 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Supplemental Oxygen
Arm Type
Active Comparator
Arm Description
Inspired oxygen fraction > 0.5 and SpO2 = 98-100%
Arm Title
Air or supplemental oxygen
Arm Type
Experimental
Arm Description
Air or lowest possible inspired concentration of oxygen to maintain SpO2 > 90%
Intervention Type
Drug
Intervention Name(s)
Oxygen
Other Intervention Name(s)
Medical oxygen
Intervention Description
Oxygen in sufficient quantity to maintain SpO2 > 98%
Intervention Type
Other
Intervention Name(s)
Air
Other Intervention Name(s)
Medical Air
Intervention Description
Supplemental Oxygen in sufficient quantity to maintain SpO2 > 90%
Primary Outcome Measure Information:
Title
Composite morbidity
Description
Major complications such as MACE, TIA/stroke/renal insufficiency/POCD etc
Time Frame
0 - 1 month postoperatively
Secondary Outcome Measure Information:
Title
Long term outcome (Major complications)
Description
Major complications
Time Frame
1 month to 1 year postoperatively
Title
Specific outcomes (Major adverse cardiac events (MACE))
Description
Major adverse cardiac events (MACE)
Time Frame
0 - 1 year postoperatively
Title
Specific outcomes (TIA or stroke)
Description
TIA or stroke
Time Frame
0 - 1 year postoperatively
Title
Specific outcomes (renal insufficiency including dialysis or renal failure)
Description
renal insufficiency including dialysis or renal failure
Time Frame
0 - 1 year postoperatively
Other Pre-specified Outcome Measures:
Title
Complication (Re-operation or bleeding)
Description
Re-operation or bleeding
Time Frame
0 - 30 days postoperatively

10. Eligibility

Sex
All
Minimum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients undergoing elective vascular surgery (peripheral or aortic surgery), No language or cognitive disability Written, informed consent Exclusion Criteria: Patients with COPD/other lung diseases that require preoperative oxygen therapy Patients undergoing carotid artery surgery
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Anil Gupta, MD, PhD
Organizational Affiliation
Örebro University, Sweden
Official's Role
Principal Investigator
Facility Information:
Facility Name
University Hospital
City
Örebro
ZIP/Postal Code
701 85
Country
Sweden
Facility Name
Örebro University Hospital
City
Örebro
ZIP/Postal Code
70185
Country
Sweden

12. IPD Sharing Statement

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Is Peri-operative Hyperoxemia a Risk Factor for Postoperative Complications?

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