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Endoscopic Findings in Iron Deficiency Anemia: A Cross-Sectional Study From Port Sudan

Endoscopic Findings in Iron Deficiency Anemia: A Cross-Sectional Study From Port Sudan

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07143435
Acronym
IDA
Enrollment
117
Registered
2025-08-27
Start date
2019-02-11
Completion date
2021-08-17
Last updated
2025-08-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Anemia, Endoscopy, Iron Deficiency Anemia

Keywords

Sudan, Gastrointestinal blood loss, Endoscopic findings

Brief summary

Background: Iron deficiency anemia (IDA) is a common condition often linked to gastrointestinal blood loss, making endoscopic evaluation essential for identifying underlying causes. This study aimed to assess the endoscopic findings in patients presenting with IDA in Red Sea State, Sudan. Understanding the prevalence and types of gastrointestinal lesions among these patients can aid in early diagnosis and management, reducing associated morbidity and mortality. By focusing on patients undergoing endoscopic evaluation, this study provides valuable insights into the burden of gastrointestinal pathologies contributing to IDA in the region. Materials and Methods: This cross-sectional, descriptive study was conducted in the Endoscopy Unit at Alkaleej Medical Complex - Portsudan. Adults aged ≥18 years with IDA undergoing endoscopic evaluation were included, excluding those unwilling participation or with incomplete data. Data were collected via structured questionnaires and medical records, covering demographics, medical history, clinical presentation, and endoscopic findings. SPSS version 26 - 2018, was used for analysis, applying descriptive statistics and chi-square tests to assess associations. Ethical approval was obtained, and informed consent was secured from all participants.

Interventions

None listed

Sponsors

National Center for Gastroentestinal and Liver Disease
Lead SponsorOTHER

Study design

Observational model
OTHER
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* Adults aged 18 years and above. * Patients diagnosed with IDA who underwent endoscopic evaluation.

Exclusion criteria

* Patients who declined to participate in the study. * Patients with incomplete medical records or missing endoscopic findings.

Design outcomes

Primary

MeasureTime frameDescription
Proportion of patients with endoscopic lesions explaining iron deficiency anemia4 monthsPercentage of participants with one or more endoscopic findings potentially accounting for IDA (e.g., gastric/duodenal ulcer, gastritis with bleeding, colonic mass/ulcer, angiodysplasia), confirmed by endoscopy ± biopsy when indicated.

Secondary

MeasureTime frameDescription
Proportion of biopsy-proven malignancies4 monthsPercentage of participants with histopathology-confirmed gastrointestinal malignancy (e.g., gastric adenocarcinoma, colorectal cancer).

Countries

Sudan

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026