Preoperative Anemia Frequency

April 10, 2023 updated by: Gamze Küçükosman, Zonguldak Bulent Ecevit University
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.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Study Type

Observational

Enrollment (Actual)

853

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

  • Turkey
      • Zonguldak, Turkey, 67600
        • Gamze Küçükosman

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult
  • Older Adult

Accepts Healthy Volunteers

N/A

Sampling Method

Non-Probability Sample

Study Population

Patients over 18 years of age, without massive bleeding, of both sexes

Description

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

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
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

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
PREOPERATIVE ANEMIA FREQUENCY AND TREATMENT APPROACH
Time Frame: Patients who applied to the outpatient clinic within a 3-month period after ethical approval
preoperative anemia frequency
Patients who applied to the outpatient clinic within a 3-month period after ethical approval

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
PREOPERATIVE ANEMIA FREQUENCY AND TREATMENT APPROACH
Time Frame: Patients who applied to the outpatient clinic within a 3-month period after ethical approval
blood transfusion frequency
Patients who applied to the outpatient clinic within a 3-month period after ethical approval

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Zonguldak Bulent Ecevit University

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

November 1, 2021

Primary Completion (Actual)

January 31, 2022

Study Completion (Actual)

January 31, 2022

Study Registration Dates

First Submitted

March 29, 2023

First Submitted That Met QC Criteria

March 29, 2023

First Posted (Actual)

April 11, 2023

Study Record Updates

Last Update Posted (Actual)

April 12, 2023

Last Update Submitted That Met QC Criteria

April 10, 2023

Last Verified

April 1, 2023

More Information

Terms related to this study

Keywords

Additional Relevant MeSH Terms

Other Study ID Numbers

  • 2021/20

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

UNDECIDED

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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