Evidence map›Paper›PMID 38276544›Full record

Trial reportNutrients2024

Efficacy and Safety of Calcifediol in Young Adults with Vitamin D Deficiency: A Phase I, Multicentre, Clinical Trial-POSCAL Study.

Pedro Guerra López, Mikel Urroz Elizalde, Noelia Vega-Gil, Blanca Sánchez Santiago, Iñaki Zorrilla Martínez, Mario Jiménez-Mercado, Esteban Jódar, Araitz Landeta Manzano, Cristina Campo Hoyos, Jesús Frías Iniesta

Open access · goldAbstract readClinical Trial, Phase IMulticenter StudyRandomized Controlled Trial
In one paragraph

Trial report in Nutrients, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
1.3field-weighted citation impact, top 23% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed, 3 citations in OpenAlex.

  1. Trial
  2. Trial
  3. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors at 6 institutions in 1 country.

Pedro Guerra LópezClinical Trials Unit, Pharmacology Department, Universidad Autónoma de Madrid, 28049 Madrid, Spain.
Mikel Urroz ElizaldeClinical Trials Unit, Pharmacology Department, Universidad Autónoma de Madrid, 28049 Madrid, Spain.ORCID 0000-0002-6951-5518
Noelia Vega-GilValdecilla Clinical Trials Unit, Hospital Universitario Marqués de Valdecilla-IDIVAL, 39008 Santander, Spain.
Blanca Sánchez SantiagoValdecilla Clinical Trials Unit, Hospital Universitario Marqués de Valdecilla-IDIVAL, 39008 Santander, Spain.ORCID 0009-0005-8077-3752
Iñaki Zorrilla MartínezClinical Trials Unit, IIS BIOARABA, 01009 Vitoria-Gasteiz, Spain.
Mario Jiménez-MercadoClinical Trials Unit, IIS BIOARABA, 01009 Vitoria-Gasteiz, Spain.ORCID 0000-0001-8248-2821
Esteban JódarDepartment of Endocrinology and Nutrition, Quirónsalud Madrid University Hospital, 28233 Madrid, Spain.
Araitz Landeta ManzanoMedical Affairs, FAES FARMA S.A., 48940 Leioa, Spain.
Cristina Campo HoyosMedical Affairs, FAES FARMA S.A., 48940 Leioa, Spain.
Jesús Frías IniestaClinical Trials Unit, Pharmacology Department, Universidad Autónoma de Madrid, 28049 Madrid, Spain.
Faes Farma (Spain) · ESHospital Universitario La Paz · ESInstituto de Investigación Marqués de Valdecilla · ESHospital Universitario Quirónsalud Madrid · ESUniversidad Autónoma de Madrid · ESUniversity of the Basque Country · ES

Funding

Faes Farma (Spain) N/A
6 · The paper itself

Abstract

Vitamin D deficiency is highly prevalent, and recent evidence suggests a possible association between vitamin D deficiency and various health conditions. The aim of this study was to assess monthly calcifediol treatments for vitamin D deficiency (or biweekly, if the deficiency was severe) in a young adult population with no associated comorbidities. This multicentre phase I trial started with a four month open-label treatment phase (TP) that included 101 participants (65% women with mean age 29.8 years). Eighty-two percent of the subjects (79/96) achieved 25(OH)D levels within the target range (20-60 ng/mL) by the end of the TP, and they were subsequently randomised and subjected to a double-blind, placebo-controlled, five month follow-up phase (FP). At the end of the FP, 89% of participants maintained vitamin D levels of >20 ng/mL with calcifediol, versus 49% with placebo (

Indexed as

CalcifediolVitamin D DeficiencyAdultDouble-Blind MethodFemaleHumansMaleVitamin DYoung AdultCalcifediolVitamin D25-hydroxyvitamin D3calcifediolclinical trialvitamin D deficiencyyoung adults

Identifiers

PMID38276544
PMCPMC10818887
OpenAlexW4391027013

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.