Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 2 de 2
Filtrar
Mais filtros

Bases de dados
País/Região como assunto
Ano de publicação
Tipo de documento
País de afiliação
Intervalo de ano de publicação
1.
Trials ; 19(1): 475, 2018 Sep 05.
Artigo em Inglês | MEDLINE | ID: mdl-30185221

RESUMO

BACKGROUND: Sciatica is a common condition reported to affect over 3% of the UK population at any time and is often caused by a prolapsed intervertebral disc (PID). Although the duration and severity of symptoms can vary, pain persisting beyond 6 weeks is unlikely to recover spontaneously and may require investigation and treatment. Currently, there is no specific care pathway for sciatica in the National Health Service (NHS), and no direct comparison exists between surgical microdiscectomy and transforaminal epidural steroid injection (TFESI). The NERVES (NErve Root block VErsus Surgery) trial aims to address this by comparing clinical and cost-effectiveness of surgical microdiscectomy and TFESI to treat sciatica secondary to a PID. METHODS/DESIGN: A total of 163 patients were recruited from NHS out-patient clinics across the UK and randomised to either microdiscectomy or TFESI. Adult patients (aged 16-65 years) with sciatic pain endured for between 6 weeks and 12 months are eligible if their symptoms have not been improved by at least one form of conservative (non-operative) treatment and they are willing to provide consent. Patients will be excluded if they present with neurological deficit or have had previous surgery at the same level. The primary outcome is patient-reported disability measured using the Oswestry Disability Questionnaire (ODQ) score at 18 weeks post randomisation and secondary outcomes include disability and pain scales using numerical pain ratings, modified Roland-Morris and Core Outcome Measures Index at 12-weekly intervals, and patient satisfaction at 54 weeks. Cost-effectiveness and quality of life (QOL) will be assessed using the EQ-5D-5 L and self-report cost data at 12-weekly intervals and Hospital Episode Statistics (HES) data. Adverse event data will be collected. Analysis will follow the principle of intention-to-treat. DISCUSSION: NERVES is the first trial to evaluate the comparative clinical and cost-effectiveness of microdiscectomy to local anaesthetic and steroid administered via TFESI. The results of this research may facilitate the development of an evidence-based treatment strategy for patients with sciatica. TRIAL REGISTRATION: ISRCTN, ID: ISRCTN04820368 . Registered on 5 June 2014. EudraCT EudraCT2014-002751-25. Registered on 8 October 2014.


Assuntos
Dor nas Costas/terapia , Discotomia/métodos , Glucocorticoides/administração & dosagem , Deslocamento do Disco Intervertebral/terapia , Microcirurgia/métodos , Bloqueio Nervoso/métodos , Ciática/terapia , Raízes Nervosas Espinhais/efeitos dos fármacos , Triancinolona/administração & dosagem , Adolescente , Adulto , Idoso , Dor nas Costas/diagnóstico , Dor nas Costas/etiologia , Dor nas Costas/fisiopatologia , Ensaios Clínicos Fase III como Assunto , Análise Custo-Benefício , Avaliação da Deficiência , Discotomia/efeitos adversos , Discotomia/economia , Custos de Medicamentos , Feminino , Glucocorticoides/efeitos adversos , Glucocorticoides/economia , Humanos , Injeções Epidurais , Deslocamento do Disco Intervertebral/complicações , Deslocamento do Disco Intervertebral/diagnóstico , Deslocamento do Disco Intervertebral/fisiopatologia , Masculino , Microcirurgia/efeitos adversos , Microcirurgia/economia , Pessoa de Meia-Idade , Estudos Multicêntricos como Assunto , Bloqueio Nervoso/efeitos adversos , Bloqueio Nervoso/economia , Medição da Dor , Qualidade de Vida , Ensaios Clínicos Controlados Aleatórios como Assunto , Recuperação de Função Fisiológica , Ciática/diagnóstico , Ciática/etiologia , Ciática/fisiopatologia , Raízes Nervosas Espinhais/fisiopatologia , Fatores de Tempo , Resultado do Tratamento , Triancinolona/efeitos adversos , Triancinolona/economia , Reino Unido , Adulto Jovem
2.
J Clin Epidemiol ; 70: 17-25, 2016 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-26169841

RESUMO

OBJECTIVES: Evaluate current data sharing activities of UK publicly funded Clinical Trial Units (CTUs) and identify good practices and barriers. STUDY DESIGN AND SETTING: Web-based survey of Directors of 45 UK Clinical Research Collaboration (UKCRC)-registered CTUs. RESULTS: Twenty-three (51%) CTUs responded: Five (22%) of these had an established data sharing policy and eight (35%) specifically requested consent to use patient data beyond the scope of the original trial. Fifteen (65%) CTUs had received requests for data, and seven (30%) had made external requests for data in the previous 12 months. CTUs supported the need for increased data sharing activities although concerns were raised about patient identification, misuse of data, and financial burden. Custodianship of clinical trial data and requirements for a CTU to align its policy to their parent institutes were also raised. No CTUs supported the use of an open access model for data sharing. CONCLUSION: There is support within the publicly funded UKCRC-registered CTUs for data sharing, but many perceived barriers remain. CTUs are currently using a variety of approaches and procedures for sharing data. This survey has informed further work, including development of guidance for publicly funded CTUs, to promote good practice and facilitate data sharing.


Assuntos
Ensaios Clínicos como Assunto/economia , Apoio Financeiro , Disseminação de Informação/métodos , Confidencialidade , Humanos , Política Organizacional , Projetos de Pesquisa , Inquéritos e Questionários , Reino Unido
SELEÇÃO DE REFERÊNCIAS
DETALHE DA PESQUISA