Evidence map›Paper›PMID 37890866›Full record

ArticleClinical and translational science2023

Evaluation of factors associated with recruitment rates in early phase clinical trials based on the European Clinical Trials Register data.

Paloma Moraga Alapont, Paula Prieto, Mikel Urroz, María Jiménez, Antonio J Carcas, Alberto M Borobia

Abstract read
In one paragraph

Article in Clinical and translational science, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
–field-weighted citation impact
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

7 citing papers in PubMed.

  1. Trial
  2. Article
  3. Article
  4. Article
  5. Exploring Parental Experiences of Childhood Ear Health Clinics and Their Acceptability of AI-Based Diagnostic Tools: A Qualitative Study.Health expectations : an international journal of public participation in health care and health policy · 2025
    Article
  6. Article
  7. Article
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

6 authors.

Paloma Moraga AlapontClinical Pharmacology Department, La Paz University Hospital, IdiPAZ, Madrid, Spain.ORCID 0009-0005-7113-7252
Paula PrietoClinical Pharmacology Department, La Paz University Hospital, IdiPAZ, Madrid, Spain.ORCID 0009-0008-5646-9664
Mikel UrrozPharmacology and Therapeutics Department, School of Medicine, Universidad Autónoma de Madrid, Madrid, Spain.ORCID 0000-0002-6951-5518
María JiménezClinical Pharmacology Department, La Paz University Hospital, IdiPAZ, Madrid, Spain.ORCID 0000-0003-4925-731X
Antonio J CarcasClinical Pharmacology Department, La Paz University Hospital, IdiPAZ, Madrid, Spain.ORCID 0000-0003-1823-4174
Alberto M BorobiaClinical Pharmacology Department, La Paz University Hospital, IdiPAZ, Madrid, Spain.ORCID 0000-0002-8584-3263

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Effective participant recruitment is a critical challenge in clinical trials. Inadequate enrollment of participants can precipitate delays, escalated costs, and compromise scientific integrity. Despite its relevance, particularly during the early phases, it persists as an obstacle in the field of clinical research. The primary aim of this study was to analyze the recruitment rates of early-phase clinical trials and evaluate their potential associations with key trial characteristics. Using a descriptive and statistical analysis, a research study was conducted based on the early-phase trials registered at the European Clinical Trials Register (EU-CTR), spanning the timeframe from January 2017 to December 2021. Among the 194 trials examined, we found median recruitment rates of 68%. A more detailed exploration revealed a greater level of success in terms of recruitment achievement in pediatric trials when compared to trials involving adults, non-oncologic trials, or those also developed in non-European countries. It is important to underscore that only 69 trials out of the total managed to conclude recruitment, with the most prevalent reason for premature cessation being the presence of efficacy and safety issues or sponsor's strategy. This number can be greatly improved. Despite certain disparities observed in the information within EU-CTR, we have successfully determined the recruitment rates of the studies and established associations with some of the clinical trial characteristics analyzed. Owing to the inherent constraints of this study, further research is warranted to gain a comprehensive understanding of the intricate interplay between trial characteristics and their impact on recruitment rates in early-phase studies.

Indexed as

Clinical Trials as TopicPatient SelectionAdultChildHumansResearch Design

Identifiers

PMID37890866
PMCPMC10719455

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.