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Effect of Folic Acid Supplementation in Pregnant Women Having Thalassaemia Trait

Primary Purpose

Thalassemia, Folic Acid Deficiency Anemia

Status
Not yet recruiting
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Folic acid
Materna
Sponsored by
The University of Hong Kong
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Thalassemia

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)FemaleAccepts Healthy Volunteers

Inclusion Criteria:

  • Singleton pregnancy
  • Alpha thalassaemia trait
  • Beta thalassaemia trait

Exclusion Criteria:

  • Women taking over 0.6mg folic acid daily for 3 months or more prior to and during pregnancy
  • Gestational age > 16 weeks at first antenatal visit
  • Women age =< 18 years old
  • Booking BMI =< 18 or >= 35
  • Serum ferritin level < 30ug/L or 68 pmol/L
  • Concomitant alpha and beta thalassaemia
  • Hb H disease
  • Beta thalassaemia major
  • Beta thalassaemia intermediate
  • Thalassaemia other than alpha or beta type
  • Women on long term medications
  • Women with risk factors for NTD
  • Women with known epilepsy
  • Women with bariatric surgery or malabsorption diseases
  • Women with known MTHFR polymorphism
  • Vegetarian

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm 3

    Arm Type

    Active Comparator

    Active Comparator

    Active Comparator

    Arm Label

    Folic acid 5mg

    Folic acid 0.5mg

    Materna

    Arm Description

    Outcomes

    Primary Outcome Measures

    Haemoglobin level
    Maternal RBC folate concentration
    Maternal serum folate concentration
    Cord blood RBC
    Cord blood serum folate concentration

    Secondary Outcome Measures

    Ferritin level
    Maternal Vitamin B12
    Cord blood vitamin B12

    Full Information

    First Posted
    March 5, 2020
    Last Updated
    May 9, 2023
    Sponsor
    The University of Hong Kong
    Collaborators
    Queen Mary Hospital, Hong Kong
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    1. Study Identification

    Unique Protocol Identification Number
    NCT04310059
    Brief Title
    Effect of Folic Acid Supplementation in Pregnant Women Having Thalassaemia Trait
    Official Title
    A Randomized Controlled Trial to Study the Effect of Folic Acid Supplementation in Pregnant Women Having Thalassaemia Trait
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    May 2022
    Overall Recruitment Status
    Not yet recruiting
    Study Start Date
    January 1, 2024 (Anticipated)
    Primary Completion Date
    December 31, 2025 (Anticipated)
    Study Completion Date
    December 31, 2026 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Sponsor
    Name of the Sponsor
    The University of Hong Kong
    Collaborators
    Queen Mary Hospital, Hong Kong

    4. Oversight

    Studies a U.S. FDA-regulated Drug Product
    No
    Studies a U.S. FDA-regulated Device Product
    No
    Data Monitoring Committee
    No

    5. Study Description

    Brief Summary
    Folic acid supplementation has been recommended for prevention of neural tube defects in pregnancy when taken periconceptionally up to 12 weeks of gestation. A daily dose of 0.4mg has been endorsed by World Health Organisation to achieve a Red blood cell (RBC) folate level of 906nmol/L (400ng/mL) for reduction of neural tube defect. Hong Kong has no policy on food fortification. Research data conducted in countries with food fortification may not be applicable. It is therefore essential to study the baseline folate status in pregnant women locally. For pregnant women with thalassaemia, they are believed to have a higher risk of folate deficiency because of an increased rate of erythropoiesis and chronic haemolysis. However, information on folate level of thalassaemia trait in pregnancy is scanty. Unmetabolized folic acid has been detected in maternal and fetal blood when daily dosage greater than 0.8-1mg was taken. In term of the dosage and duration of folic acid supplementation after 12 weeks of gestation, the practice varies widely among public hospitals and Maternity & Child Health Care centres. It is therefore essential to study the optimal dosage of folic acid supplementation in women with thalassaemia.
    Detailed Description
    Folic acid supplementation is well established for its role in prevention of neural tube defects (NTD) when taken periconceptionally up to 12 weeks of gestation. The naturally occurring form, folate, is a water soluble B vitamin (B9) that is mostly present in dark green leafy vegetables and legumes. However, it is only 50% bioavailable. Folic acid, on the contrary, as a synthetic form of folate is almost completely bioavailable especially when administered in an empty stomach. It has been endorsed by World Health Organisation that RBC folate cutoff of 906 nmol/L (400ng/mL) is required for reduction of NTD. This level is only achievable by taking Folic acid supplementation of 0.4mg/day. Women at higher risk of having recurrent NTD is recommended to take higher dose at 4mg/day. Patients with thalassaemia have an increased rate of erythropoiesis and chronic haemolysis. They are believed to have a higher rate of folate turnover and consequentially higher risk of folate deficiency. Guideline from Royal College of Obstetricians and Gynaecologists recommends daily intake of 5mg folic acid preconceptionally to prevent NTD. But, it does not specify whether this dosage is applicable to all types and degrees of thalassaemias and research data on the optimal dosage is lacking. In addition to prevention of NTD, the supplementation of folic acid is also recommended for pregnant thalassaemia women for prevention of antenatal anaemia. In a retrospective study of Chinese population reported in 1989, women with beta-thalassaemia minor taking additional 5mg folic acid had higher pre-delivery haemoglobin concentration of 10.1 g/dL compared to haemoglobin level of 9.7 g/dL in the group taking Obimin (a pregnancy supplement containing 0.25mg folic acid and 90 mg ferrous fumarate). However, there was no further randomised controlled trial to validate this observation. Though a higher folic acid supplementation was believed to be beneficial in prevention of antenatal anaemia, unmetabolized folic acid were detected in maternal and fetal blood when daily dosage greater than 0.8-1mg was taken. Moreover, a higher rate of urinary excretion of folic acid was also observed in pregnant women receiving higher dosage of folic acid supplementation. In non-pregnant beta thalassaemia major patients, folic acid supplementation at 1 mg daily was advised as cessation of which could lead to a significant reduction in serum folate. This has been counter-proposed by the observation of normal to high serum folate levels in transfusion dependent thalassaemia receiving optimal transfusion. Indeed, folic acid supplementation should be considered for non-transfusion dependent thalassaemia as excessive erythropoiesis is required to maintain satisfactory haemoglobin. Folate level drops during pregnancy to puerperal period. Information on folate level of thalassaemia trait in pregnancy is scanty. In a paper published in 1985, no difference in serum folate was found between normal women and women with thalassaemia trait, and hence usual supplementation was suggested. Hong Kong has no policy on food fortification. Research data conducted in countries with food fortification may not be applicable. The folate status may have been changed in last few decades because of better general nutritional status and public knowledge of preconception folic acid supplementation. The preparation of 5mg folic acid is available in all public hospitals and preparation of 0.5mg folic acid is recently introduced. As such, the 5mg folic acid prescription is traditionally adopted and this can be a result of its availability. However, the practice varies widely among public hospitals and Maternity & Child Health Care centres. There is no standardised guideline on the dosage and indications of folic acid supplementation for pregnant thalassaemic women. More importantly, no recent data on the baseline folate status in pregnant women with thalassaemia is available locally. Patient blood management in Obstetrics has been advocated with an aim to minimize blood loss by maintaining haemoglobin levels, reduce blood transfusion and optimize patient outcome. Identification and treatment of maternal anaemia is one of the three main pillars to achieve it. Even though thalassaemia can be considered as a risk factor for NTD, it remains controversial as to how much folic acid supplementation is adequate for pregnant women with thalassaemia trait in prevention of maternal anaemia which is a key element in maternity care.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Thalassemia, Folic Acid Deficiency Anemia

    7. Study Design

    Primary Purpose
    Prevention
    Study Phase
    Not Applicable
    Interventional Study Model
    Parallel Assignment
    Masking
    None (Open Label)
    Allocation
    Randomized
    Enrollment
    270 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    Folic acid 5mg
    Arm Type
    Active Comparator
    Arm Title
    Folic acid 0.5mg
    Arm Type
    Active Comparator
    Arm Title
    Materna
    Arm Type
    Active Comparator
    Intervention Type
    Dietary Supplement
    Intervention Name(s)
    Folic acid
    Intervention Description
    women will be randomised into one of the three groups. Group A - Folic acid 5mg/day Group B - Folic acid 0.5mg/day Group C - Materna one tablet/day (a pregnancy supplement containing 0.6mg folic acid)
    Intervention Type
    Dietary Supplement
    Intervention Name(s)
    Materna
    Intervention Description
    Materna
    Primary Outcome Measure Information:
    Title
    Haemoglobin level
    Time Frame
    Change in level throughout the pregnancy, up to 42 weeks
    Title
    Maternal RBC folate concentration
    Time Frame
    Change in level throughout the pregnancy, up to 42 weeks
    Title
    Maternal serum folate concentration
    Time Frame
    Change in level throughout the pregnancy, up to 42 weeks
    Title
    Cord blood RBC
    Time Frame
    Upon birth
    Title
    Cord blood serum folate concentration
    Time Frame
    Upon birth
    Secondary Outcome Measure Information:
    Title
    Ferritin level
    Time Frame
    Change in level throughout the pregnancy, up to 42 weeks
    Title
    Maternal Vitamin B12
    Time Frame
    Maternal Vitamin B12 at first antenatal visit
    Title
    Cord blood vitamin B12
    Time Frame
    Cord blood vitamin B12 upon birth

    10. Eligibility

    Sex
    Female
    Gender Based
    Yes
    Gender Eligibility Description
    Only pregnant women are recruited
    Minimum Age & Unit of Time
    18 Years
    Accepts Healthy Volunteers
    Accepts Healthy Volunteers
    Eligibility Criteria
    Inclusion Criteria: Singleton pregnancy Alpha thalassaemia trait Beta thalassaemia trait Exclusion Criteria: Women taking over 0.6mg folic acid daily for 3 months or more prior to and during pregnancy Gestational age > 16 weeks at first antenatal visit Women age =< 18 years old Booking BMI =< 18 or >= 35 Serum ferritin level < 30ug/L or 68 pmol/L Concomitant alpha and beta thalassaemia Hb H disease Beta thalassaemia major Beta thalassaemia intermediate Thalassaemia other than alpha or beta type Women on long term medications Women with risk factors for NTD Women with known epilepsy Women with bariatric surgery or malabsorption diseases Women with known MTHFR polymorphism Vegetarian
    Central Contact Person:
    First Name & Middle Initial & Last Name or Official Title & Degree
    Pui Wah Hui, MD
    Phone
    852-22553402
    Email
    apwhui@hku.hk

    12. IPD Sharing Statement

    Plan to Share IPD
    No
    Citations:
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    7474275
    Citation
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    Effect of Folic Acid Supplementation in Pregnant Women Having Thalassaemia Trait

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