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Completed

NCT Number: NCT03952533

α-lipoic Acid (ALA), Magnesium, Vitamin B6 and Vitamin D and Risk Factor for Pre-term Birth

Effects of oral administration of a food supplement constituted by α-lipoic acid, magnesium, vitamin B6 and vitamin D in tablets of 1,2 g administered daily to women presenting risk factors for preterm birth (PTB). The aim is to reduce the rate of short cervix at 19-21 weeks of gestational age and consequently reduce the occurrence of PTB.

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Key information

Age range

18 year–41 year

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

University of Modena and Reggio Emilia

Modena, Mo, 41100, Italy

About this study

The physiological course of pregnancy can be threatened by the onset of rhythmic and progressive uterine contractions, associated with a shortening and dilation of the cervix.

These modifications occur as a consequence of inflammatory processes that involve important changes in the extracellular matrix of connective tissues. For this reason, in the event of a threat of preterm birth, the appropriate tocolytic therapies should be associated with interventions able to counteract morphological changes in the uterine cervix. Women presenting high or low BMI, presence of uterine myomas, metrorrhagia during the first trimester and hypertensive disorders are at risk for PTB. Current management practices remain profoundly various, without a therapeutic tocolytic strategy, especially because most of the first-line tocolytic drugs used present important side effects [8]. It is to be assessed whether a supplementation during pregnancy with minerals, vitamins, anti-inflammatory and anti-oxidant agents can avoid PTB in women with risk factors.

ALA may interact synergistically with magnesium, vitamin B6 and vitamin D, limiting some of the main factors related to the risk of preterm delivery - probably via the inhibition of nuclear factor k beta (NF-kB)-signaling pathway - and reducing therefore the rate of uterine contractions.

Moreover, the administration of ALA, magnesium, vitamin B6 and vitamin D have been demonstrated to be safe in pregnancy.

The aim of the present study is to evaluate whether pregnant women presenting risk factors for PTB, treated with a combination of ALA, magnesium, vitamin 6 and vitamin D from 11-14 weeks of gestational age, until delivery, could present a reduced rate of cervical shortening measured by transvaginal ultrasound (TVS) at 11-14 weeks and 19-21 weeks of gestational age.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Nulliparous,
  • Previous History of preterm birth,
  • Age between 18 - 41 years,
  • 11-14 weeks of gestation,
  • BMI < 18 kg/m2 or ≥ 30 kg/m2,
  • Uterine myoma,
  • Hypertensive disorders either chronic or induced by the pregnancy

Exclusion criteria

  • PPROM,
  • Cervical dilation ≥ 1 cm

Treatment and study plan

Dav

Dietary Supplement

Daily oral administration of a food supplement constituted by α-lipoic acid, magnesium, vitamin B6 and vitamin D in tablets of 1,2 g (Dav®, Lo.Li. Pharma, Rome, Italy)

Primary outcomes

  1. Cervical shortening

    Time frame: from 11-14 weeks to 19-21 weeks of Gestational age

    Cervical shortening detected by the transvaginal ultrasound (TVS)

  2. Rate of Short Cervix

    Time frame: at 19-21 weeks of Gestational age

    Rate of cervical length < 25mm at the TVS exam

  3. Rate of Preterm birth

    Time frame: from 11-14 weeks to 37 weeks of Gestational age

    Number of preterm birth occurred

Secondary outcomes

  1. Accesses to the ET for Threatened PTB

    Time frame: from 11-14 weeks to 37 weeks of Gestational age

    Number of accesses to the ER for threatened PTB due to episodes of preterm uterine contractions and/or cervical shortening

  2. Maternal hospitalization for threatened preterm labor

    Time frame: from 11-14 weeks to 37 weeks of Gestational age

    Maternal need for hospital admission for threatened preterm labor

Sponsors and collaborators

Lead sponsor

University of Modena and Reggio Emilia

Other

Registry information

Official study title

Effects of the Supplementation of α-lipoic Acid (ALA), Magnesium, Vitamin B6 and Vitamin D to Women Presenting Risk Factor for Pre-term Birth

Acronym: ALA

Important dates

Study start
2019
Primary completion
2020
Study completion
2021
First posted
May 16, 2019
Registry last updated
May 18, 2022

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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