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Awareness of Iron Status Evaluation in UGIB (AISE)

H

Hat Yai Medical Education Center

Status

Completed

Conditions

Upper Gastrointestinal Bleeding

Study type

Observational

Funder types

Other

Identifiers

NCT06299007
HYH EC 052-66-01 (Other Grant/Funding Number)

Details and patient eligibility

About

BACKGROUND: Data on the awareness of the need to evaluate iron status and IDA prevalence in acute UGIB are limited.

OBJECTIVES: This study aimed to investigate the rate of evaluation of iron status and prevalence of iron deficiency anemia (IDA) and the associated factors in patients with anemia hospitalized for acute upper gastrointestinal bleeding (UGIB).

Enrollment

867 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • patients > 18 years of age who were admitted because of acute UGIB and were diagnosed with anemia from UGIB during hospitalization.

Exclusion criteria

  • patients who had previously undergone endoscopy at another institution before admission
  • patients who had a definite cause of UGIB that was inconclusive
  • incomplete data for analysis.

Trial design

867 participants in 1 patient group

Group 1
Description:
Patients who were admitted due to upper gastrointestinal bleeding and had anemia

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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