Skip to main content
Clinical Trials/EUCTR2006-001710-32-DK
EUCTR2006-001710-32-DK
Active, not recruiting
Not Applicable

PeRioperative OXygen fraction – effect on surgical site Infection and pulmonary complications after abdominal surgery. (The PROXI-study) - The PROXI-study

Dept. of Anaesthesia, Centre of Head and Orthopaedics, Copenhagen University Hospital Rigshospitalet0 sites1,400 target enrollmentJune 21, 2006
Conditionsaparotomy

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
aparotomy
Sponsor
Dept. of Anaesthesia, Centre of Head and Orthopaedics, Copenhagen University Hospital Rigshospitalet
Enrollment
1400
Status
Active, not recruiting
Last Updated
13 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
June 21, 2006
End Date
TBD
Last Updated
13 years ago
Study Type
Interventional clinical trial of medicinal product
Sex
All

Investigators

Sponsor
Dept. of Anaesthesia, Centre of Head and Orthopaedics, Copenhagen University Hospital Rigshospitalet

Eligibility Criteria

Inclusion Criteria

  • Age 18 years or older.
  • Laparotomy, acute or elective. In case of gynaecological surgery only if malignancy is suspected (defined as risk of ovarian malignancy index \>200 or a specimen with atypic or neoplastic cells).
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1\.2 Adults (18\-64 years) yes
  • F.1\.2\.1 Number of subjects for this age range
  • F.1\.3 Elderly (\>\=65 years) yes
  • F.1\.3\.1 Number of subjects for this age range

Exclusion Criteria

  • Surgery within 30 days before scheduled laparotomy (except surgery in local anaesthesia)
  • Chemotherapy within 3 months
  • Inability to give informed consent
  • Inability to keep oxygen saturation above 90% without supplemental oxygen (measured preoperatively by pulseoximetry)

Outcomes

Primary Outcomes

Not specified

Similar Trials