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临床试验/NCT07366502
NCT07366502招募中不适用

Comprehensive Hematological and Biochemical Comparison of Low-Dose Liposomal Iron Versus Standard-Dose Conventional Oral Iron in Iron Deficiency Anemia Following Sleeve Gastrectomy: A Prospective, Randomized Clinical Trial

Medeni Şermet1 个研究点 分布在 1 个国家目标入组 70 人开始时间: 2025年9月1日最近更新:
干预措施

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
70
试验地点
1
主要终点
Change in Hemoglobin Level From Baseline to Week 24

研究概览

简要总结

Low-dose liposomal iron (17-34 mg elemental/day) was compared with standard conventional oral iron (100-200mg elemental/day) in the treatment of iron deficiency anemia following sleeve gastrectomy. Liposomal iron provided superior hematological improvement and gastrointestinal tolerance.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Single (Participant)

入排标准

年龄范围
18 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Age between 18 and 65 years
  • History of laparoscopic sleeve gastrectomy performed at least 6 months prior to enrollment
  • Diagnosis of iron deficiency anemia, defined as:
  • Hemoglobin <12 g/dL in women or <13 g/dL in men, and
  • Serum ferritin <30 ng/mL or transferrin saturation (TSAT) <20%
  • Mild to moderate anemia (hemoglobin ≥9 g/dL)
  • Ability to take and swallow oral medications
  • Willingness to participate and provide written informed consent

排除标准

  • Active gastrointestinal disease (e.g., inflammatory bowel disease, peptic ulcer disease, or gastrointestinal bleeding)
  • Chronic kidney disease with estimated GFR <30 mL/min/1.73 m²
  • Use of oral or parenteral iron, vitamin B12, or folate supplementation within the previous 3 months
  • Iron overload or hemochromatosis (serum ferritin >300 ng/mL)
  • Known allergy or intolerance to iron preparations
  • Active malignancy
  • Pregnancy or breastfeeding
  • Known hemoglobinopathies (e.g., thalassemia, sickle cell disease)
  • Blood transfusion within the previous 1 month
  • Cognitive or psychiatric disorder interfering with study participation or protocol adherence

研究组 & 干预措施

Arm 2 Title: Conventional Iron (Group KD)

Active Comparator

Participants with iron deficiency anemia after laparoscopic sleeve gastrectomy receiving conventional oral ferrous iron preparations.

干预措施: conventional oral iron (Drug)

Arm 1 Title: Liposomal Iron (Group LD)

Experimental

Participants with iron deficiency anemia after laparoscopic sleeve gastrectomy receiving oral liposomal iron.

干预措施: Liposomal Iron (Drug)

结局指标

主要结局

Change in Hemoglobin Level From Baseline to Week 24

时间窗: 24 weeks

The change in hemoglobin concentration will be calculated as the absolute difference between baseline and week 24 values.

次要结局

  • Change in Serum Ferritin Level From Baseline to Week 24(24 weeks)
  • Change in Transferrin Saturation (TSAT) From Baseline to Week 24(24 weeks)
  • Change in Serum Iron Level From Baseline to Week 24(24 weeks)

研究者

发起方
Medeni Şermet
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Medeni Şermet

assoc.prof., MD.

Goztepe Prof Dr Suleyman Yalcın City Hospital

研究点 (1)

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