Prediction of Morbidity and Mortality With Medical Pre-Operative Fitness Assessment

Sponsor
Assiut University (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05892796
Collaborator
(none)
122
18

Study Details

Study Description

Brief Summary

Aim to measure the predictability of medical pre -Operative Fitness Assessment to the actual rates of morbidity and mortality related to surgery in Assiut university Hospital.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    Perioperative morbidity and mortality remain the mostly important barrier to surgical interventions worldwide. Therefor, decision making relies upon accurate risk Assessment to be balanced with hoped benefit.

    For elective surgeries, multiple clinical tools have been used to Assessment perioperative Fitness, but with limited applicability. For instance, the american society of anesthesiologists phesical status score (ASA-PS) does not consider the type of surgery, nor the patient's age.

    The physiological and Operative severity score for the enumeration of mortality (POSSUM) evaluates the intra-operative difficulties, limiting the preoperative prediction.

    Recently, researchers layer and his colleagues at University Hospital Bonn, modified the preoperative score to Predict Postoperative Mortality (POSPOM) to be applied in daily practice.

    In investigator 's practice, Assiut university Hospitals already have a Pre-Operative Fitness Assessment (POFA) clinical and investigator aim to adapt and evaluate the POSPOM system in investigator' s practice.

    Study Design

    Study Type:
    Observational
    Anticipated Enrollment :
    122 participants
    Observational Model:
    Cohort
    Time Perspective:
    Prospective
    Official Title:
    Prediction of Morbidity and Mortality With Medical Pre-Operative Fitness Assessment
    Anticipated Study Start Date :
    Jun 1, 2023
    Anticipated Primary Completion Date :
    Sep 1, 2024
    Anticipated Study Completion Date :
    Dec 1, 2024

    Outcome Measures

    Primary Outcome Measures

    1. Incidance of 22 adverse events according to the Eurepian perioperative clinical outcom definitions [Baseline]

      Follow up of preoperative medically diseased patients after surgery to detect outcoms

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 75 Years
    Sexes Eligible for Study:
    All
    Inclusion Criteria:
    • Adults (>18 years old ) preparing for elective intervention.
    Exclusion Criteria:
    • those who do not require anaesthesia Those who did not undergo surgery

    Contacts and Locations

    Locations

    No locations specified.

    Sponsors and Collaborators

    • Assiut University

    Investigators

    None specified.

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    Responsible Party:
    Yasmeen Abdelshafy Ebrahim, Investigator, Assiut University
    ClinicalTrials.gov Identifier:
    NCT05892796
    Other Study ID Numbers:
    • mPOFA
    First Posted:
    Jun 7, 2023
    Last Update Posted:
    Jun 7, 2023
    Last Verified:
    May 1, 2023
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by Yasmeen Abdelshafy Ebrahim, Investigator, Assiut University

    Study Results

    No Results Posted as of Jun 7, 2023