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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.
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).
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Lactoferrin enriched-yogurt | Experimental | In this arm participants were randomized to receved a lactoferrin-enriched yogurt (100mg/125g) twice a day for two months. |
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| Non-enriched yogurt | Other | In this arm participants were randomized to received a non-enriched yogurt(125g) twice a day for two months. |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Lactoferrin-enriched yogurt supplementation | Dietary Supplement | Women were randomized to receive the lactoferrin-enriched yogurt (experimental arm, n=25) - (100mg/125g) 2 times a day for 2 months.Yogurt derived from high-quality cow's milk, with the same color, flavor, and texture as the control group yogurt not enriched with lactoferrin. All women of the group received nutritional guidance in accordance with dietary guidelines that accounted for the macronutrient contribution provided by 250g/day of yogurt. The products were provided in unlabeled white plastic cups, distinguishable only by a unique code. |
| Measure | Description | Time Frame |
|---|---|---|
| Change in serum ferritin levels after consumption of lactoferrin-enriched yogurt compared to the non-enriched control yogurt. | 8 weeks - The change in serum ferritin concentration was assessed from baseline to the end of the intervention period. |
| Measure | Description | Time Frame |
|---|---|---|
| Changes in Hemoglobin concentration. (HGB) [g/dL] | The unit of measure for hemoglobin concentration is grams per deciliter (g/dL). | 8 weeks |
| Occurrence of adverse maternal outcomes [number and percentage of participants] |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Simona Bo, Associate Professor, MD | University of Turin, Italy | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| AOU Città della Salute e della Scienza di Torino, University of Torino, Torino. | Torino | Torino | 10126 | Italy |
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| Type | Includes Protocol | Includes SAP | Includes ICF | Document Label | Document Date | Document Uploaded Date | Document File Name |
|---|---|---|---|---|---|---|---|
| ICF | No | No | Yes | Informed Consent Form | Jan 16, 2023 | Dec 11, 2025 | ICF_000.pdf |
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| ID | Term |
|---|---|
| D016640 | Diabetes, Gestational |
| ID | Term |
|---|---|
| D011248 | Pregnancy Complications |
| D005261 | Female Urogenital Diseases and Pregnancy Complications |
| D000091642 | Urogenital Diseases |
| D003920 | Diabetes Mellitus |
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| Non-enriched yogurt | Dietary Supplement | Participants were randomized to receved a non-enriched yogurt (125g)- (control arm) twice a day for 2 months. The yogurt was produced from high-quality semi-skimmed cow's milk and It was identical in color, taste, texture, and packaging to the experimental yogurt which conteins lactoferrin. The products were provided in unlabeled white plastic cups, distinguishable only by a unique code. |
|
The unit of measure is the number and percentage (%) of participants with at least one adverse maternal event (yes/no).
| 8 weeks |
| Changes in Hematocrit values. (HCT) [%] | The unit of measure for hematocrit values is percent (%). | 8 weeks |
| Changes in Red Blood Cells count. (RBC) [×10⁶/µL] | The unit of measure for red blood cell count is ×10⁶ per microliter (µL). | 8 WEEKS |
| Changes in serum Iron levels. [µg/dL] | The unit of measure for serum iron levels is micrograms per deciliter (µg/dL). | 8 weeks |
| Changes in Transferrin levels. [mg/dL] | The unit of measure for transferrin levels is milligrams per deciliter (mg/dL). | 8 weeks |
| Change in Total Iron-Binding Capacity (TIBC) [µg/dL] | The unit of measure for TIBC is micrograms per deciliter (µg/dL) | 8 weeks |
| Change in Transferrin Saturation. [%] | The unit of measure for transferrin saturation is percent (%). | 8 weeks |
| Change in fasting blood glucose concentration (metabolic variables) [mg/dL] | The unit of measure for glucose concentration is milligrams per deciliter (mg/dL). | 8 weeks |
| Change in fasting serum insulin levels (metabolic variables) [mIU/L] | The unit of measure for insulin is milli-international units per liter (mIU/L). | 8 weeks |
| Occurrence of adverse neonatal outcomes [number and percentage of participants] | The unit of measure is the number and percentage (%) of neonates with at least one adverse neonatal outcome (yes/no). | At delivery |
| Changes in the maternal gut microbiota composition. [%] | The unit of measure is the relative abundance (%) of bacterial taxa identified by 16S rRNA gene sequencing. | 8 weeks |
| D044882 | Glucose Metabolism Disorders |
| D008659 | Metabolic Diseases |
| D009750 | Nutritional and Metabolic Diseases |
| D004700 | Endocrine System Diseases |