Retrospective Evaluation of the Effect of Iron (Fe) Infusion on Complications in Anemic Patients Undergoing Thoracotomy

Sponsor
Ankara University (Other)
Overall Status
Completed
CT.gov ID
NCT05673161
Collaborator
(none)
220
1
30
223.2

Study Details

Study Description

Brief Summary

In patients who underwent thoracotomy due to lung malignancy; It is desired to investigate whether there is a difference in terms of postoperative results between those with and without anemia, and those with iron deficiency anemia (IDA) who underwent intravenous iron replacement and those who did not, according to the hemoglobin value in their preoperative examinations.

Condition or Disease Intervention/Treatment Phase
  • Other: iron

Study Design

Study Type:
Observational
Actual Enrollment :
220 participants
Observational Model:
Other
Time Perspective:
Retrospective
Official Title:
Retrospective Evaluation of the Effect of Iron (Fe) Infusion on Complications in Anemic Patients Undergoing Thoracotomy
Actual Study Start Date :
Nov 15, 2022
Actual Primary Completion Date :
Dec 15, 2022
Actual Study Completion Date :
Dec 15, 2022

Arms and Interventions

Arm Intervention/Treatment
anemia, treatment

anemic patients who had iron therapy

Other: iron
iron treatment

anemia, no treatment

anemic patients who had no therapy

Outcome Measures

Primary Outcome Measures

  1. number of patients who had postoperatiive complication [3 days]

    postoperative complication

  2. number of patients who received blood products [3 days]

    use of blood product

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 85 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • thoracotomy patients
Exclusion Criteria:
  • emergency cases

Contacts and Locations

Locations

Site City State Country Postal Code
1 Ankara University Ankara Turkey

Sponsors and Collaborators

  • Ankara University

Investigators

  • Principal Investigator: CIGDEM YILDIRIM GUCLU, Ankara University

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
CIGDEM YILDIRIM GUCLU, Assoc Prof Dr, Ankara University
ClinicalTrials.gov Identifier:
NCT05673161
Other Study ID Numbers:
  • 2022/613
First Posted:
Jan 6, 2023
Last Update Posted:
Jan 6, 2023
Last Verified:
Jan 1, 2023
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
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 Jan 6, 2023