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The OK Daily Study

Oral Vitamin K2 (Menaquinone-7; MK-7) Supplementation and Effect on Vitamin K Status of Breastfed Term Infants in Early Infancy; a Four-cohort Prospective, Part-randomised, Part-blinded Study.

The OK Daily Study is a multi-centred, part-randomised, part blinded, four cohort study. We are exploring daily dietary supplementation with vitamin K2, specifically menaquinone-7 (MK-7), given to breastfed infants or breastfeeding mothers to see whether this improves the incidence of biochemical vitamin K deficiency in the infants at 2 months postnatal age.

The overall aims are:

  • To compare infant MK-7 supplementation with placebo
  • To compare maternal MK-7 supplementation with placebo
  • To compare infant MK-7 supplementation and maternal MK-7 supplementation
  • To compare infant MK-7 supplementation with vitamin K1 supplementation via infant formula milk.

Once recruited, mother and infant pairs will be grouped initially based on the families' feeding choice. Breastfed infants will then be randomised 2:1 to the infant supplementation or maternal supplementation group. Within the infant supplementation group, infants will either receive MK-7 with vitamin D or a placebo containing vitamin D.

Follow up will occur at 2 months postnatal age (range 2-3 months postnatal age), where bloods and breastmilk samples will be collected to assess the infant and maternal vitamin K status.

研究概览

详细说明

The OK Daily Study is a multi-centre study taking place in the Norfolk and Norwich University Hospital, Norwich, UK, and Ashford and St Peters' Hospital, Chertsey, UK.

Infants born at ≥37 weeks' gestation will be recruited in the participating site if they meet eligibility criteria and are born within the recruitment window. Recruitment will take place before the mother and infant are discharged from the hospital following birth.

The two main arms of this study are breastfeeding and formula feeding. Mother and infant pairs will initially be allocated based on the family's feeding preferences.

Infants in the breastfeeding arm will be randomised into group 1 or group 2 in a 2:1 ratio. Group 1 allocation will be blinded; group 2 allocation will be open label.

  • Group 1 - infant supplementation group. Infants will receive either 45 micrograms/day of MK-7 with 10 micrograms/day vitamin D3 or a placebo consisting of 10 micrograms/day vitamin D3
  • Group 2 - maternal supplementation group. Mothers in this group will receive 2 mg/day MK-7. All breastfeeding infants in this group will receive 10 micrograms/day of vitamin D3.

Formula fed infants will be in group 3 and will not require any additional supplementation as part of this study. This is because infant formula is already supplemented with adequate amounts of vitamin K1 and vitamin D.

All supplements will be started within 7 days of birth. Vitamin D drops are included for breastfed infants as per national UK guidelines.

Follow up will be as follows:

  • 1 month postnatal visit (range 1-1.5 months) - phone call.

    o Confirmation of eligibility to continue, assessment of compliance with the intervention, and to schedule the in person follow up visit

  • 2 months postnatal (range 2-3 months) - in person visit.

    • All babies will have a single blood sample taken.
    • Mothers who are in group 2 (mothers who have had MK-7 supplementation) and a selection of mothers from group 1 (breastfeeding mothers who are not supplemented with MK-7) will have a single blood sample taken and will be asked to provide a single breastmilk sample
    • Mothers will be asked about their opinions on practising the supplementation.

Blood samples will be analysed for vitamin K status, including Proteins Induced by Vitamin K Absence/antagonism of prothrombin (PIVKA-II) and of osteocalcin (undercarboxylated osteocalcin), dephosphorylated-undercarboxylated matrix gla-protein (dp-ucMGP) and serum vitamin K concentrations (including of vitamin K1 and MK-7). Breastmilk samples will be analysed for vitamin K concentrations (including vitamin K1 and MK-7)

Once this in person follow up visit has been completed, the mother and baby pair will have completed the study.

研究类型

介入性

注册 (估计的)

134

阶段

  • 不适用

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习联系方式

研究联系人备份

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

  • 孩子

接受健康志愿者

是的

描述

Inclusion Criteria:

  • Infants, and mothers of infants, born ≥37 weeks gestational age
  • Standard dose of intramuscular (IM) vitamin K prophylaxis given to the neonate following birth
  • For breastfeeding mothers: the mother intends to exclusively/predominantly breastfeed their baby for at least 2 months

Exclusion Criteria:

  • Inability or refusal to provide informed consent
  • Inability to adhere to or comply with study procedures
  • Babies who meet the inclusion gestation but would otherwise, as part of routine neonatal care, be provided with daily vitamin K drops (i.e. NeoKay drops) at discharge
  • IM vitamin K prophylaxis not received at birth (parents declined vitamin K prophylaxis or parents chose for neonate to receive an oral course of vitamin K prophylaxis instead)
  • Evidence of conjugated hyperbilirubinaemia (these babies are at higher risk of VKDB)
  • Mothers, and babies born to mothers, who are taking any medication that could affect or antagonise vitamin K metabolism (i.e. warfarin, the anti-epileptic drugs phenytoin or carbamazepine, and cephalosporin, rifampicin and isoniazid antimicrobials)

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

  • 主要用途:预防
  • 分配:随机化
  • 介入模型:并行分配
  • 屏蔽:单身的

武器和干预

参与者组/臂
干预/治疗
其他:Mother and infant pairs who are breastfeeding.

Group 1 = infant supplementation group. Infants in this group will be randomised to receive either 6 drops a day containing 45 micrograms/day of MK-7 plus 10 micrograms/day vitamin D3 OR 10 micrograms/day vitamin D3 only (the active placebo, containing no vitamin K)

Group 2 = maternal supplementation group. Mothers in this group will be given 2 mg/day MK-7 capsules. Infants in this group will receive 10 micrograms/day vitamin D3.

6 drops/day providing 45 micrograms/day MK-7 plus 10 micrograms/day of vitamin D3
其他名称:
  • Vitamin K2 supplemented infant group
6 drops/day providing 10 micrograms/day vitamin D3 and no supplementary MK-7.
其他名称:
  • Vitamin K2 unsupplemented group
1 mg capsules of menaquinone-7, with a daily dose of 2 mg (i.e. 2 capsules per day)
有源比较器:Formula Feeding Infants
Infants who are exclusively formula feeding. These infants will receive the recommended daily amount of vitamin K through their formula milk intake and so will not receive any additional vitamin K supplementation.
6 drops/day providing 10 micrograms/day vitamin D3 and no supplementary MK-7.
其他名称:
  • Vitamin K2 unsupplemented group

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
Comparison of the proportion of participants who have a PIVKA-II >0.05 AU/mL in the unsupplemented and supplemented infants.
大体时间:2 months postnatal age (range 2-3 months).

PIVKA-II = protein induced by vitamin K antagonism/absence; clotting protein II.

Measured via serum blood sample in arbitrary units/mL. For the primary outcome, this is the comparison between the supplemented and unsupplemented infants.

2 months postnatal age (range 2-3 months).

次要结果测量

结果测量
措施说明
大体时间
Comparison of the proportion of participants who have a PIVKA-II >0.05 AU/mL in the various study groups.
大体时间:2 months postnatal age (range 2-3 months).

PIVKA-II = protein induced by vitamin K antagonism/absence; clotting protein II.

Measured via serum blood sample in arbitrary units/mL. For secondary outcome, this is comparison between remaining groups, other than those assessed in the primary outcome measure.

2 months postnatal age (range 2-3 months).
Comparison of serum levels of osteocalcin (undercarboxylated and carboxylated) between the study groups.
大体时间:2 months postnatal age (range 2-3 months).
Both undercarboxylated and carboxylated levels of osteocalcin will be measured in nanograms/mL.
2 months postnatal age (range 2-3 months).
Comparison of the percentage of undercarboxylated osteocalcin as a proportion of total osteocalcin (%GluOC) between the study groups.
大体时间:2 months postnatal age (range 2-3 months).
Total osteocalcin calculated by the sum of the undercarboxylated and carboxylated osteocalcin values.
2 months postnatal age (range 2-3 months).
Comparison of serum levels of dephosphorylated undercarboxylated matrix Gla Protein in included participants between the study groups.
大体时间:2 months postnatal age (range 2-3 months).
Measured in picomol/mL
2 months postnatal age (range 2-3 months).
Comparison of levels of serum K vitamers (including, but no limited to, vitamin K1 and menaquinone-7) between the study groups.
大体时间:2 months postnatal age (range 2-3 months).
Serum K vitamers will be reported in micrograms/mL.
2 months postnatal age (range 2-3 months).
Comparison of the levels of breastmilk K vitamers (including, but not limited to, vitamin K1 and menaquinone-7) between unsupplemented and supplemented mothers.
大体时间:2 months postnatal age (range 2-3 months).
Serum K vitamers will be reported in nanograms/mL
2 months postnatal age (range 2-3 months).
Investigation of percentage compliance to study supplementation.
大体时间:2 months postnatal age (range 2-3 months).
Amount of remaining supplement will be assessed at follow up. This will then be used to calculate percentage compliance by comparing it to the expected volumes.
2 months postnatal age (range 2-3 months).
Investigation regarding families' opinions about infant and maternal vitamin supplementation.
大体时间:2 months postnatal age (range 2-3 months).
Measured via verbal questioning at follow up.
2 months postnatal age (range 2-3 months).

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

调查人员

  • 首席研究员:Paul Clarke, Professor、Norfolk and Norwich University Hospitals NHS Foundation Trust

出版物和有用的链接

负责输入研究信息的人员自愿提供这些出版物。这些可能与研究有关。

一般刊物

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始 (估计的)

2026年10月1日

初级完成 (估计的)

2027年9月1日

研究完成 (估计的)

2028年8月1日

研究注册日期

首次提交

2026年5月13日

首先提交符合 QC 标准的

2026年5月27日

首次发布 (实际的)

2026年6月2日

研究记录更新

最后更新发布 (实际的)

2026年9月4日

上次提交的符合 QC 标准的更新

2026年9月1日

最后验证

2026年9月1日

更多信息

此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.

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