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临床试验/NCT07287384
NCT07287384已完成不适用

Effects of a Dairy Product Enriched With Lactoferrin on Iron Status of Women With Gestational Diabetes. A Pilot Randomized Controlled Double-blind Trial

University of Turin, Italy2 个研究点 分布在 1 个国家目标入组 50 人开始时间: 2023年3月1日最近更新:

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
50
试验地点
2
主要终点
Change in serum ferritin levels after consumption of lactoferrin-enriched yogurt compared to the non-enriched control yogurt.

研究概览

简要总结

This pilot double-blind, randomized controlled trial with two parallel arms, was performed to evaluate the change in serum ferritin concentration following consumption of lactoferrin enriched yogurt versus the non-enriched control yogurt in women with GDM.

详细描述

Lactoferrin is recognized as both effective and safe during pregnancy. Nonetheless, studies specifically investigating its effects in women with GDM are limited.

The primary outcome of this pilot RCT was the change in serum ferritin concentration following the consumption of lactoferrin-enriched yogurt compared with non-enriched control yogurt. Secondary outcomes included changes between the two arms in hemoglobin concentration, hematocrit, red blood cell count, serum iron, transferrin levels, total iron-binding capacity, and transferrin saturation. Additional outcomes were the evaluation of variations in metabolic variables, the occurrence of adverse maternal and neonatal outcomes, and changes in the maternal gut microbiota before and after the intervention

The study began on March 1, 2023, and continued until May 31, 2025. All participants with diagnosis of GDM were recruited according to the inclusion criteria.

Participants received the same dietary counseling and nutritional recommendations aligned with current guidelines by trained registered dieticians. Women were randomized to receive the lactoferrin-enriched yogurt (experimental arm, n=25) and the non-enriched control yogurt (control arm, n=25). Both products were derived from high-quality cow's milk, had the same color, flavor, texture, and were contained in identical unlabeled white 125g plastic cups, each identified solely by a code. The experimental product was enriched with lactoferrin during the manufacturing process (100mg/125g).

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
Triple (Participant, Care Provider, Investigator)

入排标准

年龄范围
18 Years 至 50 Years(Adult)
性别
Female
接受健康志愿者

入选标准

  • Diagnosis of GDM confirmed by 75g glucose oral glucose tolerance test (OGTT).
  • Caucasian ethnicity, gestational age between 24 and 30 weeks.
  • Age >18 and <50 years.
  • Body Mass Index (BMI) between 22.5 and 35 kg/m².
  • Ability to provide informed consent to participate in the study.

排除标准

  • Type 1 diabetes mellitus.
  • Allergies to milk proteins or lactose intolerance.
  • Known anemia.
  • Twin pregnancy.
  • Pre-existing iron supplementation exceeding 30 mg/day.
  • Insulin therapy at the time of enrollment.
  • Any condition or disease requiring specific dietary treatments.
  • Concurrent physical or mental conditions requiring pharmacological therapy
  • Autoimmune disorders.

结局指标

主要结局

Change in serum ferritin levels after consumption of lactoferrin-enriched yogurt compared to the non-enriched control yogurt.

时间窗: 8 weeks - The change in serum ferritin concentration was assessed from baseline to the end of the intervention period.

次要结局

  • Changes in Hemoglobin concentration. (HGB) [g/dL](8 weeks)
  • Occurrence of adverse maternal outcomes [number and percentage of participants](8 weeks)
  • Changes in Hematocrit values. (HCT) [%](8 weeks)
  • Changes in Red Blood Cells count. (RBC) [×10⁶/µL](8 WEEKS)
  • Changes in serum Iron levels. [µg/dL](8 weeks)
  • Changes in Transferrin levels. [mg/dL](8 weeks)
  • Change in Total Iron-Binding Capacity (TIBC) [µg/dL](8 weeks)
  • Change in Transferrin Saturation. [%](8 weeks)
  • Change in fasting blood glucose concentration (metabolic variables) [mg/dL](8 weeks)
  • Change in fasting serum insulin levels (metabolic variables) [mIU/L](8 weeks)
  • Occurrence of adverse neonatal outcomes [number and percentage of participants](At delivery)
  • Changes in the maternal gut microbiota composition. [%](8 weeks)

研究者

发起方
University of Turin, Italy
申办方类型
Other
责任方
Principal Investigator
主要研究者

Simona Bo

Associate Professor

University of Turin, Italy

研究点 (2)

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