Evidence map›Paper›PMID 37069219›Full record

ReviewCommunications medicine2023

The importance of appropriate selection of clinical endpoints in outpatient COVID-19 clinical trials.

Kristian Thorlund, Davey Smith, Christopher Linsell, Nicholas White, Christopher Butler, David Boulware, Judith Currier, Ofir Harari, Edouard Lhomme, Nathalie Strub-Wourgaft and 2 more

Abstract readReview
In one paragraph

Review in Communications medicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
  4. Article
  5. 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

12 authors.

Kristian ThorlundMcMaster University, Hamilton, Canada.
Davey SmithSchool of Health Sciences, University of California San Diego, San Diego, CA, USA.
Christopher LinsellVanderbilt Institute for Clinical and Translational Research (VICTR) Methods Program, Vanderbilt University, Nashville, TN, USA.ORCID http://orcid.org/0000-0002-3297-2811
Nicholas WhiteNuffield Department of Medicine, Centre for Tropical Medicine and Global Health, University of Oxford, Oxford, UK.
Christopher ButlerNuffield Department of Primary Care Health Sciences, University of Oxford, Oxford, UK.
David BoulwareUniversity of Minnesota Medical School, Minneapolis, MN, USA.ORCID http://orcid.org/0000-0002-4715-0060
Judith CurrierUCLA Division of Infectious Diseases, Department of Medicine, University of California Los Angeles, Los Angeles, CA, USA.ORCID http://orcid.org/0000-0003-4279-4737
Ofir HarariCytel, Vancouver, Canada.
Edouard LhommeHospital Center University De Bordeaux, Bordeaux, France.
Nathalie Strub-WourgaftDrugs for Neglected Diseases Initiative, Geneva, Switzerland.
Stacey AdamFoundation for the National Institutes of Health, North Bethesda, MD, USA.
Edward MillsMcMaster University, Hamilton, Canada. millsej@mcmaster.ca.

Funding

Medical Research Council MC_PC_19079
6 · The paper itself

Abstract

Clinical trial endpoints must be carefully and intentionally selected so that the results of the trial can be used to inform policy- and decision-making. The relative importance of potential endpoints often depends on the stakeholder, with patients having different preferences to policymakers and regulators. The set up of clinical trials for COVID-19 was problematic, as endpoints that could be reasonably measured did not always match the efficacy endpoints usually required by guideline panels. Thus, different endpoints were used, which made the timely comparison and evaluation of interventions difficult. Here we discuss the evolution of the COVID-19 landscape and the effect this is having on the selection of consistent and measurable clinical trial endpoints. Using appropriate endpoints is crucial for researchers to offer the most reliable, valid, and interpretable results possible.

Identifiers

PMID37069219
PMCPMC10107578

What OpenQuestion holds

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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.