Literature DB >> 16790737

The future of neonatal therapeutic trials.

T Stephenson1, H Budge.   

Abstract

Neonatology has undoubtedly benefited from clinical trials. Nevertheless, more treatments based on inadequate experimental evidence are given than those that are supported by a validated evidence base. Clinicians seeking the basis for their current and future clinical practice are faced with challenges in the shadow of recent UK legislation and government recommendations. All patients must be protected from inappropriate research, but the benefits of regulations must be appropriately balanced with those of properly conducted clinical trials. It is ethically difficult both to persist with treatments of unproven benefit and unknown harm and to deny infants potentially valuable therapies. It is important that trials are conducted within the new legislative framework, but their future may rest with innovative solutions and the determination of all involved in the process.

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Year:  2006        PMID: 16790737      PMCID: PMC2672739          DOI: 10.1136/adc.2005.076802

Source DB:  PubMed          Journal:  Arch Dis Child Fetal Neonatal Ed        ISSN: 1359-2998            Impact factor:   5.747


  6 in total

1.  Support for studies in paediatric medicine is needed.

Authors:  R Lennon; M Quinn; K Collard
Journal:  BMJ       Date:  2000-11-11

2.  Who is speaking for children and adolescents and for their health at the policy level?

Authors:  A Aynsley-Green; M Barker; S Burr; A Macfarlane; J Morgan; J Sibert; T Turner; R Viner; T Waterston; D Hall
Journal:  BMJ       Date:  2000-07-22

Review 3.  Medicines for children--the last century and the next.

Authors:  T Stephenson
Journal:  Arch Dis Child       Date:  2001-09       Impact factor: 3.791

4.  Unlicensed and off label drug use in neonates.

Authors:  S Conroy; J McIntyre; I Choonara
Journal:  Arch Dis Child Fetal Neonatal Ed       Date:  1999-03       Impact factor: 5.747

5.  Government sets up inquiry into ventilation trial.

Authors:  Judy Jones
Journal:  BMJ       Date:  1999-02-27

6.  Directive 2001/20/EC of the European Parliament and of the Council of 4 April 2001 on the approximation of the laws, regulations and administrative provisions of the member states relating to the implementation of good clinical practice in the conduct of clinical trials on medicinal products for human use.

Authors: 
Journal:  Med Etika Bioet       Date:  2002 Spring-Summer
  6 in total

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