Preoperative Anemia Frequency

Sponsor
Zonguldak Bulent Ecevit University (Other)
Overall Status
Completed
CT.gov ID
NCT05808283
Collaborator
(none)
853
1
3
285.3

Study Details

Study Description

Brief Summary

In our retrospective study, it was aimed to determine the frequency of anemia in non-emergency patients over the age of 18 who applied to the Anesthesiology and Reanimation Department of our hospital.

Condition or Disease Intervention/Treatment Phase
  • Other: preoperative anemia frequency

Study Design

Study Type:
Observational
Actual Enrollment :
853 participants
Observational Model:
Other
Time Perspective:
Prospective
Official Title:
Preoperative Anemia Frequency
Actual Study Start Date :
Nov 1, 2021
Actual Primary Completion Date :
Jan 31, 2022
Actual Study Completion Date :
Jan 31, 2022

Arms and Interventions

Arm Intervention/Treatment
Those with anemia according to WHO definition (Group 1)

Other: preoperative anemia frequency
patients who applied to the outpatient clinic prospectively for 3 months
Other Names:
  • blood transfusion frequency
  • Those without anemia according to WHO definition (Group 2)

    Other: preoperative anemia frequency
    patients who applied to the outpatient clinic prospectively for 3 months
    Other Names:
  • blood transfusion frequency
  • Outcome Measures

    Primary Outcome Measures

    1. PREOPERATIVE ANEMIA FREQUENCY AND TREATMENT APPROACH [Patients who applied to the outpatient clinic within a 3-month period after ethical approval]

      preoperative anemia frequency

    Secondary Outcome Measures

    1. PREOPERATIVE ANEMIA FREQUENCY AND TREATMENT APPROACH [Patients who applied to the outpatient clinic within a 3-month period after ethical approval]

      blood transfusion frequency

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Inclusion Criteria:
    • -patient over 18 years old,

    • Patients applying to the Department of Anesthesiology and Reanimation AD

    Exclusion Criteria:
    • Pregnant,

    • under 18 years old,

    • will undergo cardiac and emergency surgery

    • Patients with Massive Bleeding

    • Patients who underwent multiple surgeries during the study period

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Gamze Küçükosman Zonguldak Turkey 67600

    Sponsors and Collaborators

    • Zonguldak Bulent Ecevit University

    Investigators

    None specified.

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Gamze Küçükosman, medical doctor, Zonguldak Bulent Ecevit University
    ClinicalTrials.gov Identifier:
    NCT05808283
    Other Study ID Numbers:
    • 2021/20
    First Posted:
    Apr 11, 2023
    Last Update Posted:
    Apr 12, 2023
    Last Verified:
    Apr 1, 2023
    Individual Participant Data (IPD) Sharing Statement:
    Undecided
    Plan to Share IPD:
    Undecided
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by Gamze Küçükosman, medical doctor, Zonguldak Bulent Ecevit University
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Apr 12, 2023