Intraoperative Oxygen Concentration on Incidence of Surgical Site Infection

Sponsor
Assiut University (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT06108791
Collaborator
(none)
100
2
14

Study Details

Study Description

Brief Summary

Surgical site infections (SSI) are the most common healthcare-associated infections and sources of morbidity and over-mortality. Factors that have been proven to reduce SSI include antimicrobial prophylaxis, maintenance of perioperative normothermia, avoidance of hyperglycemia, proper surgical techniques, and adequate pain relief postoperatively

Condition or Disease Intervention/Treatment Phase
N/A

Detailed Description

In 2016, a systematic review and meta-analysis assessing the effects of systematic high FiO2 (80%) compared with standard FiO2 (30%) concluded that high FiO2 was associated with a reduction of SSI in patients undergoing surgery under general anesthesia. Consequently, the WHO recommended that "adult patients undergoing general anesthesia should receive an 80% FiO2 intra-operatively to reduce the risk of SSI".These recommendations have sparked a large debate on the benefits and harms of hyperoxemia. From the theoretical point-of-view, several pro (prevention of hypoxemia, SSI, and postoperative nausea and vomiting) and con (respiratory adverse events, increased production of harmful "reactive oxygen species") arguments have been raised by believers and detractors of high FiO2. Accordingly, and despite these recommendations, anesthetists still used a wide range of intraoperative FiO2 in daily practice and frequently changed FiO2 settings during surgery unrelated to patients' PaO2 or SpO2.

The PROXI study, the largest multicenter randomized controlled trial specifically designed to assess the role of high vs. low intraoperative FiO2 on SSI, did not report any reduction of the incidence of SSI with the administration of 80% FiO2 during colorectal surgery. Similarly, the recent multicenter randomized iPROVE-O2 trial that included 740 patients undergoing major abdominal surgery, ventilated intraoperatively with an evidence-based protective strategy, reported a similar SSI rate between the 30% and 80% FiO2 groups.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
100 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Double (Participant, Outcomes Assessor)
Primary Purpose:
Prevention
Official Title:
High vs Low Inspired Intraoperative Oxygen Concentration on the Incidence of Surgical Site Infection in Hepatobiliary Surgeries
Anticipated Study Start Date :
Jan 1, 2024
Anticipated Primary Completion Date :
Jan 1, 2025
Anticipated Study Completion Date :
Mar 1, 2025

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: HIGH FIO2

will include 50 patients: each one will receive intraoperatively a high concentration of oxygen (80% oxygen + 20% air), following extubation, high-concentration oxygen supplementation will be maintained and given through non-rebreathing face mask with a reservoir at 10 L/min for 2 h.

Drug: FIO2=0.8
the concentration of intraoperative inspired fraction of oxygen is 80% oxygen + 20% air

Placebo Comparator: LOW FIO2

will include 50 patients: each one will receive intraoperatively standard concentration oxygen (33% oxygen + 66% air) followed by oxygen supplementation through the standard Venturi face mask of 30%

Drug: FIO2=0.33
the concentration of intraoperative inspired fraction of oxygen is 33% oxygen + 66% air

Outcome Measures

Primary Outcome Measures

  1. Incidence of SSI [30 DAYS]

    - the incidence of SSI postoperatively according to the Centers for Disease Control (CDC) criteria up to 30 days

Secondary Outcome Measures

  1. Pulmonary complications [14 days]

    defined as the need for controlled ventilation or arterial oxygen saturation below 90% despite supplemental oxygen.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 80 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
    • BMI of <35 kg/m2
  • scheduled for elective abdominal laparotomy/ laparoscopy under general anesthesia with an expected surgical time longer than 2 h.

  • ASA I and II

Exclusion Criteria:
    • Patients undergoing minor procedures, where the expected duration of surgery will be less than 1 hour.
  • emergency surgeries for bowel obstruction.

  • abdominal surgery for vascular or plastic indications.

  • patients with a recent history of fever,

  • patients with uncontrolled diabetes mellitus,

  • patient with known immunological dysfunction (on steroids, decompensated liver disease, HIV, etc.).

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • Assiut University

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Shimaa Abbas Hassan, lecturer, Assiut University
ClinicalTrials.gov Identifier:
NCT06108791
Other Study ID Numbers:
  • SSI32641
First Posted:
Oct 31, 2023
Last Update Posted:
Oct 31, 2023
Last Verified:
Oct 1, 2023
Individual Participant Data (IPD) Sharing Statement:
Yes
Plan to Share IPD:
Yes
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Oct 31, 2023