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OpenTrials
Completed

NCT Number: NCT02494271

TIVA, Inhalation Anesthesia, and Surgical Site Infection

The purpose of this retrospective study was to evaluate the incidence of SSI after colorectal surgery under the general anesthesia by different general anesthetic technique: inhalation versus total intravenous anesthesia.

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Key information

Conditions

Colorectal Disorders

Age range

20 year–90 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Seoul National University Bundang Hospital

Seongnam-si, Gyeonggi-do, 463-707, South Korea

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Adult patients who underwent elective colorectal surgery under general anesthesia from January 2011 to December 2013.

Exclusion criteria

  • None

Treatment and study plan

Primary outcomes

  1. Surgical site infection

    Time frame: Postoperative 30 day

    Number of participants with surgical site infection

Secondary outcomes

  1. Postoperative C-reactive protein

    Time frame: Postoperative 1 day

    Plasma concentration

  2. Segmented neutrophil count

    Time frame: Preoperaitve 1 day, postoperative 1 day

    Segmented neutrophil count

  3. Transfusion

    Time frame: The day of operation, postoperative 30 day

    Number of unit of transfused red blood cells

Sponsors and collaborators

Lead sponsor

Seoul National University Bundang Hospital

Other

Registry information

Important dates

Study start
2015
Primary completion
2015
Study completion
2015
First posted
Jul 10, 2015
Registry last updated
Jul 13, 2015

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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