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Randomised Ambulatory Management of Primary Pneumothorax (RAMPP): protocol of an open-label, randomised controlled trial.
Hallifax, Rob; Laskawiec-Szkonter, Magda; Dobson, Melissa; Gerry, Stephen; Miller, Robert F; Harvey, John E; Rahman, Najib.
Afiliação
  • Hallifax R; Department of Respiratory Medicine, Oxford University Hospitals NHS Foundation Trust, Oxford, UK.
  • Laskawiec-Szkonter M; Oxford Respiratory Trials Unit, University of Oxford, Oxford, UK.
  • Dobson M; Oxford Respiratory Trials Unit, University of Oxford, Oxford, UK.
  • Gerry S; Oxford Respiratory Trials Unit, University of Oxford, Oxford, UK.
  • Miller RF; Centre for Statistics in Medicine, University of Oxford, Oxford, UK.
  • Harvey JE; Institute for Global Health, University College London Institute of Epidemiology and Health Care, London, UK.
  • Rahman N; Department of Respiratory Medicine, North Bristol NHS Trust, Bristol, UK.
BMJ Open Respir Res ; 6(1): e000403, 2019.
Article em En | MEDLINE | ID: mdl-31179004
ABSTRACT

Introduction:

Pneumothorax is a common clinical problem. Primary spontaneous pneumothorax (PSP) occurs in otherwise fit young patients, but optimal management is not clearly defined and often results in a long hospital stay. Ambulatory treatment options are available, but the existing data on their efficacy are poor. The Randomised Ambulatory Management of Primary Pneumothorax trial is a multicentre, randomised controlled trial comparing ambulatory management with standard care, specifically designed to safely and effectively reduce hospital stay. Methods and

analysis:

236 patients with PSP will be recruited from UK hospitals. Patients will be randomised 11 to treatment to either the 'Intervention' arm (ambulatory device; Rocket Pleural Vent) or the 'Control' arm (aspiration ± standard chest drain insertion). Patients will be followed up for a total of 12 months to assess recurrence rates. The primary outcome is total length of stay in hospital (including readmissions) up to 30 days postrandomisation. The secondary outcomes are pain and breathlessness scores, air leak measurement and radiological evidence (on CT scanning) of emphysema-like changes, compared with short-term and long-term outcomes, respectively, and health economic analysis. Ethics and dissemination The trial has received ethical approval from the National Research Ethics Service Committee South-Central Oxford A (15/SC/0240). Trial registration number ISRCTN79151659.
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Texto completo: 1 Eixos temáticos: Pesquisa_clinica Base de dados: MEDLINE Assunto principal: Pneumotórax / Projetos de Pesquisa / Ensaios Clínicos Controlados Aleatórios como Assunto Tipo de estudo: Clinical_trials Limite: Humans Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Eixos temáticos: Pesquisa_clinica Base de dados: MEDLINE Assunto principal: Pneumotórax / Projetos de Pesquisa / Ensaios Clínicos Controlados Aleatórios como Assunto Tipo de estudo: Clinical_trials Limite: Humans Idioma: En Ano de publicação: 2019 Tipo de documento: Article