Predictors and Outcomes of Intraoperative Hypothermia in Patients Undergoing Knee Arthroplasty

Sponsor
Aga Khan University (Other)
Overall Status
Completed
CT.gov ID
NCT04575246
Collaborator
(none)
286
24

Study Details

Study Description

Brief Summary

The study is designed to retrospectively assess the risk factors associated with intra-operative hypothermia in patients undergoing total knee arthroplasty from January 2016 to December 2017 at Aga Khan University and also understand it's impact on post-operative outcomes.

Condition or Disease Intervention/Treatment Phase

    Study Design

    Study Type:
    Observational
    Actual Enrollment :
    286 participants
    Observational Model:
    Other
    Time Perspective:
    Cross-Sectional
    Official Title:
    Predictors and Outcomes of Intraoperative Hypothermia in Patients Undergoing Total Knee Arthroplasty: A Retrospective Cross-sectional Study From a Developing Country
    Actual Study Start Date :
    Jan 1, 2016
    Actual Primary Completion Date :
    Dec 31, 2017
    Actual Study Completion Date :
    Dec 31, 2017

    Outcome Measures

    Primary Outcome Measures

    1. Surgical Site Infection (SSI) [2016-2017]

      Post-operative infection caused total knee arthroplasty

    2. Post-operative hypothermia [Within an hour after surgery]

      Body temperature after surgery when patient is in the recovery room.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Inclusion Criteria:
    • All adults greater than 18 years who underwent total knee arthroplasty.
    Exclusion Criteria:
    • Any patient below 18 years

    Contacts and Locations

    Locations

    No locations specified.

    Sponsors and Collaborators

    • Aga Khan University

    Investigators

    None specified.

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Anum Sadruddin, Research Associate, Aga Khan University
    ClinicalTrials.gov Identifier:
    NCT04575246
    Other Study ID Numbers:
    • 2019-1274-3270
    First Posted:
    Oct 5, 2020
    Last Update Posted:
    Oct 8, 2020
    Last Verified:
    Oct 1, 2020
    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 8, 2020