Evidence map›Paper›PMID 34183329›Full record

ArticleBMJ global health2021

Algorithm for the support of non-related (serious) adverse events in an Ebola vaccine trial in the Democratic Republic of the Congo.

Gwen Lemey, Ynke Larivière, Trésor Matuvanga Zola, Vivi Maketa, Junior Matangila, Patrick Mitashi, Peter Vermeiren, Séverine Thys, Jessie De Bie, Hypolite Mavoko Muhindo and 3 more

2 registry-linked trialsAbstract read
In one paragraph

Article in BMJ global health, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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.

NCT06844487 phase3active not recruitingnot on this mapstarted 2025, after this paper: background citation

Phase 3, Randomised Maternal and Infant (From 4 to 24 Months of Age) Safety and Immunogenicity Trial of MVA-BN® Vaccine in the Democratic Republic of the Congo

TypeinterventionalSponsorJean-Pierre Van geertruydenRan2025 to 2027Enrolled344ConditionsMpox (Monkeypox), Vaccination, Immunogenicity, SafetyArmsMVA-BN standard regimen, MVA-BN half-dose regimen
NCT06844500 phase3active not recruitingnot on this mapstarted 2025, after this paper: background citation

Phase 3, Randomised Maternal and Infant (From 4 to 24 Months of Age) Safety and Immunogenicity Trial of MVA-BN® Vaccine in the Democratic Republic of the Congo

TypeinterventionalSponsorJean-Pierre Van geertruydenRan2025 to 2027Enrolled359ConditionsNeonate, Maternal Transmission, Mpox, VaccinationArmsMVA-BN standard regimen, MVA-BN standard regimen (Administered as PEP)
3 · Its place in the literature

Who cites it

6 citing papers in PubMed.

  1. Trial
  2. Trial
  3. Article
  4. Article
  5. Article
  6. 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

13 authors.

Gwen LemeyGlobal Health Institute, University of Antwerp, Antwerpen, Belgium Gwen.lemey@uantwerpen.be.ORCID 0000-0002-2879-5330
Ynke LarivièreGlobal Health Institute, University of Antwerp, Antwerpen, Belgium.ORCID 0000-0002-5422-0194
Trésor Matuvanga ZolaTropical Medicine Department, University of Kinshasa, Kinshasa, Democratic Republic of the Congo.ORCID 0000-0002-5830-415X
Vivi MaketaTropical Medicine Department, University of Kinshasa, Kinshasa, Democratic Republic of the Congo.ORCID 0000-0002-9007-1376
Junior MatangilaTropical Medicine Department, University of Kinshasa, Kinshasa, Democratic Republic of the Congo.ORCID 0000-0002-9025-3604
Patrick MitashiTropical Medicine Department, University of Kinshasa, Kinshasa, Democratic Republic of the Congo.ORCID 0000-0002-6589-2869
Peter VermeirenGlobal Health Institute, University of Antwerp, Antwerpen, Belgium.ORCID 0000-0001-6220-535X
Séverine ThysGlobal Health Institute, University of Antwerp, Antwerpen, Belgium.ORCID 0000-0001-7936-3194
Jessie De BieGlobal Health Institute, University of Antwerp, Antwerpen, Belgium.ORCID 0000-0001-9035-1549
Hypolite Mavoko MuhindoTropical Medicine Department, University of Kinshasa, Kinshasa, Democratic Republic of the Congo.ORCID 0000-0002-3307-3324
Raffaella RavinettoDepartment of Public Health, Institute of Tropical Medicine Antwerp, Antwerp, Belgium.ORCID 0000-0001-7765-2443
Pierre Van DammeCentre for the Evaluation of Vaccination, University of Antwerp, Antwerpen, Belgium.ORCID 0000-0002-8642-1249
Jean-Pierre Van GeertruydenGlobal Health Institute, University of Antwerp, Antwerpen, Belgium.ORCID 0000-0001-5006-6364

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Implementing an Ebola vaccine trial in a remote area in the Democratic Republic of the Congo (DRC), and being confronted with a dysfunctional health care system and acute unmet health needs of participants, ethical considerations were made regarding the ancillary care obligations of the sponsor and researchers. Spurred by the occurrence of non-related (serious) adverse events (NR-SAEs), the Universities of Antwerp and Kinshasa jointly developed an algorithm, accompanied by an algorithm policy. The algorithm consists of a set of consecutive questions with binary response options, leading to structured, non-arbitrary and consistent support and management for each NR-SAE. It is the result of dialogue and collaboration between the sponsor (University of Antwerp) and the principal investigator (University of Kinshasa), consultation of literature, and input of research ethics and social sciences experts. The characteristics of the project and its budgetary framework were taken into account, as well as the local socioeconomic and healthcare situation. The algorithm and related policy have been approved by the relevant ethics committee (EC), so field implementation will begin when the study activities resume in November 2021. Lessons learnt will be shared with the relevant stakeholders within and outside DRC.If NR-SAEs are not covered by a functioning social welfare system, sponsors and researchers should develop a feasible, standardised and transparent approach to the provision of ancillary care. National legislation and contextualised requirements are therefore needed, particularly in low/middle-income countries, to guide researchers and sponsors in this process. Protocols, particularly of clinical trials conducted in areas with 'access to care' constraints, should include adequate ancillary care arrangements. Furthermore, it is essential that local ECs systematically require ancillary care provisions to enhance the well-being and protection of the rights of research participants. This project was funded by the European Union's Horizon 2020 research and innovation programme, European Federation of Pharmaceutical Industries and Associations, and the Coalition for Epidemic Preparedness Innovations.

Indexed as

Ebola VaccinesHemorrhagic Fever, EbolaAlgorithmsDemocratic Republic of the CongoHumansUniversitiesEbola Vaccinesclinical trialhealth insurancehealth policypublic health

Identifiers

PMID34183329
PMCPMC8240587

What OpenQuestion holds

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LicenceCC BY-NC
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Registered trials

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.