- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT07699393
Pilot Study of Prenatal Choline Supplementation
11. juli 2026 opdateret af: Sandra W. Jacobson, Ph.D, Wayne State University
A Randomized, Double-Blind, Placebo-controlled Clinical Trial of Choline Supplementation During Pregnancy to Mitigate Adverse Effects of Prenatal Alcohol Exposure on Growth and Cognitive Development: Pilot Arm for Non-Drinking Women
A double-blind, randomized, placebo-controlled trial (RCT; NCT04395196) of prenatal choline supplementation is ongoing (1) to assess the effectiveness of maternal choline supplementation during pregnancy to mitigate effects of PAE on three primary outcomes: infant recognition memory and postnatal growth restriction (weight and head circumference); (2) to assess the efficacy of this supplementation for mitigating alcohol effects on the following secondary outcomes: infant eyeblink conditioning, postnatal length, and information processing speed.
The study design was based on a pilot feasibility study in 70 heavy-drinking pregnant women.
Infants in the choline-treated arm were more likely to meet criterion for eyeblink conditioning than those in the placebo arm.
Infants born to both the choline- and placebo-treated mothers were small at birth, but those in the choline arm showed considerable catch-up growth in weight and head circumference by 6.5 months, which persisted through 12 months.
At 12 months, infants in the choline arm showed markedly better recognition memory compared to placebo-treated on the Fagan Test of Infant Intelligence, which is known to have predictive validity for school-age IQ.
Of note, infants with heavy prenatal alcohol exposure whose mothers were in the active choline treatment arm performed better on FTII novelty preference neurobehavioral testing than infants in an observational study that was running in parallel who had no prenatal alcohol exposure.
These pilot findings indicate that any beneficial effects of prenatal choline supplementation seen may be due in part or entirely due to general beneficial effects on fetal brain development rather than mechanisms that are specific to the teratogenic effects of alcohol.
Thus, the aim of this pilot study is to enroll and randomize 50 alcohol-abstaining pregnant women to participate in an identical study protocol (same study procedures and primary and secondary outcomes) to NCT04395196, which includes only alcohol-consuming pregnant women.
Effect sizes between this pilot, non-drinking group and the larger study of alcohol-consuming women will be compared to explore the degree to which prenatal choline supplementation benefits growth and neurobehavior in infants without prenatal alcohol exposure and to explore the degree to which beneficial treatment effects of choline are specific to prenatal alcohol exposure.
Studieoversigt
Status
Rekruttering
Betingelser
Intervention / Behandling
Detaljeret beskrivelse
The study protocol will be identical to NCT04395196 except for sample size (goal = 50 pregnant women and their infants) and that instead of including heavy-drinking pregnant women, inclusion criteria require that women have fully abstained from alcohol during pregnancy at the time of randomization.
All other inclusion/exclusion criteria and study procedures are identical.
Undersøgelsestype
Interventionel
Tilmelding (Anslået)
50
Fase
- Fase 2
Kontakter og lokationer
Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.
Studiekontakt
- Navn: Sandra W Jacobson, PhD
- Telefonnummer: +13139935454
- E-mail: sandra.jacobson@wayne.edu
Undersøgelse Kontakt Backup
- Navn: R. Colin Carter, MD, MMSc
- Telefonnummer: +12123052995
- E-mail: rcc2142@cumc.columbia.edu
Studiesteder
-
-
-
Cape Town, Sydafrika
- Rekruttering
- University of Cape Town
-
Kontakt:
- Anthea Van Wyk
- Telefonnummer: +27665643491
- E-mail: uctmoms@gmail.com
-
Kontakt:
- Ernesta M Meinjtes, PhD
- E-mail: ernesta.meintjes@gmail.com
-
-
Deltagelseskriterier
Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.
Berettigelseskriterier
Aldre berettiget til at studere
- Voksen
Tager imod sunde frivillige
Ja
Beskrivelse
Inclusion Criteria:
- Age ≥18 yr
- ≤20 wk gestation
- Singleton pregnancy
- Abstinence from alcohol since conception (by report)
- Current choline dietary intake <1 g/day
- Language fluency in English or Afrikaans
Exclusion Criteria:
- Use of methamphetamine or other illicit drugs other than marijuana during the past year
- HIV positive
- Pharmacologic treatment for a serious pre-existing medical condition (e.g., diabetes, hypertension, epilepsy, or cardiac problems)
- Having another child enrolled in the trial from a previous pregnancy
- Plans for mother or child to move away from the area prior to study completion
Studieplan
Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Behandling
- Tildeling: Randomiseret
- Interventionel model: Parallel tildeling
- Maskning: Firedobbelt
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
|---|---|
|
Placebo komparator: Placebo
Placebo identisk med aktiv behandling i udseende, smag og lugt.
|
Leveres i drikkevareform
|
|
Eksperimentel: High-dose choline supplementation
2 g choline cation per day
|
Provided in beverage form.
|
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Spædbarnsgenkendelseshukommelse
Tidsramme: 12 måneder
|
Nyhedspræference fra Fagan Test of Infant Intelligence
|
12 måneder
|
|
Postnatal spædbørns vægtøgning
Tidsramme: 6,5 måneder
|
6,5 måneder
|
|
|
Postnatal vækst i spædbarnets hovedomkreds
Tidsramme: 6,5 måneder
|
6,5 måneder
|
Sekundære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Spædbørns informationsbehandlingshastighed
Tidsramme: 12 måneder
|
Behandlingshastighed på Fagan Test of Infant Intelligence
|
12 måneder
|
|
Postnatal vækst i spædbarnslængde
Tidsramme: 6,5 måneder
|
6,5 måneder
|
Samarbejdspartnere og efterforskere
Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.
Sponsor
Efterforskere
- Ledende efterforsker: Sandra W Jacobson, PhD, Wayne State University
- Ledende efterforsker: Joseph L Jacobson, PhD, Wayne State University
- Ledende efterforsker: R. Colin Carter, MD, MMSc, Columbia University
- Ledende efterforsker: Ernesta M Meinjtes, PhD, University of Cape Town
Datoer for undersøgelser
Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.
Studer store datoer
Studiestart (Anslået)
8. juli 2026
Primær færdiggørelse (Anslået)
15. oktober 2027
Studieafslutning (Anslået)
15. maj 2028
Datoer for studieregistrering
Først indsendt
6. juli 2026
Først indsendt, der opfyldte QC-kriterier
6. juli 2026
Først opslået (Faktiske)
13. juli 2026
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
14. juli 2026
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
11. juli 2026
Sidst verificeret
1. juli 2026
Mere information
Begreber relateret til denne undersøgelse
Nøgleord
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
- UCTCHOLINERCTPHASEB
Plan for individuelle deltagerdata (IPD)
Planlægger du at dele individuelle deltagerdata (IPD)?
JA
IPD-planbeskrivelse
We will share deidentified data with researchers and regulatory bodies who request the data for verification of findings, for collaboration, and/or for research purposes deemed ethical and scientifically justified by the PIs.
IPD-delingstidsramme
We will share data as described above after publication of the main findings.
IPD-delingsadgangskriterier
Requests should be made to the principle investigators.
IPD-deling Understøttende informationstype
- STUDY_PROTOCOL
- SAP
- ANALYTIC_CODE
Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter
Studerer et amerikansk FDA-reguleret lægemiddelprodukt
Ingen
Studerer et amerikansk FDA-reguleret enhedsprodukt
Ingen
Disse oplysninger blev hentet direkte fra webstedet clinicaltrials.gov uden ændringer. Hvis du har nogen anmodninger om at ændre, fjerne eller opdatere dine undersøgelsesoplysninger, bedes du kontakte register@clinicaltrials.gov. Så snart en ændring er implementeret på clinicaltrials.gov, vil denne også blive opdateret automatisk på vores hjemmeside .
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