Probiotic Use in Oral Iron Replacement Deficiency Anemia Patients Initiating Oral Iron Replacement

NCT06521879 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 295

Last updated 2024-07-26

No results posted yet for this study

Summary

Investigation of gastrointestinal tolerability, treatment compliance and iron status markers in patients with iron deficiency anemia who received oral iron replacement therapy with versus without concomitant probiotic supplementation

Conditions

Interventions

DIETARY_SUPPLEMENT

Lactobacillus plantarum 299v probiotic support

Addition of Lactobacillus plantarum 299v (L. plantarum 299v) probiotic supplementation to iron replacement therapy.

Sponsors & Collaborators

  • Antalya Training and Research Hospital

    lead OTHER_GOV

Principal Investigators

  • Gokhan Koker, MD · Antalya Training and Research Hospital

  • Yasin Sahinturk, MD · Antalya Training and Research Hospital

  • Gulhan Ozcelik Koker, MD · Antalya Training and Research Hospital

  • Ali Coskuner, MD · Antalya Training and Research Hospital

  • Merve Eren Durmuş, MD · Antalya Training and Research Hospital

  • Mutlu M Catli, MD · Antalya Training and Research Hospital

  • Ayhan H Cekin, MD · Antalya Training and Research Hospital

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2022-09-01
Primary Completion
2023-07-01
Completion
2023-07-01

Countries

  • Turkey (Türkiye)

Study Locations

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06521879 on ClinicalTrials.gov