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OpenTrials
Completed

NCT Number: NCT01807975

Forced Oscillation Versus Spirometry in Diagnosing Post Pulmonary Transplant Bronchiolitis Obliterans Syndrome

A study to evaluate the role of forced oscillation in precocious diagnosis of bronchiolitis obliterans syndrome in patients with pulmonary transplant (time difference in detecting distal airways functional impairment by forced oscillation and the standard technique using spirometry).

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Hôpital FOCH

Suresnes, Île-de-France Region, 92150, France

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patients of more than 18 year-old.
  • Patients with cardiopulmonary transplant or bilateral lung transplant.
  • Clinically stable patients

Exclusion criteria

  • Patients already diagnosed with bronchiolitis obliterans.
  • Respiratory infection.
  • Acute graft rejection.
  • Mechanical complications (bronchial dehiscence, pneumothorax, pleural effusion).
  • Iatrogenic pneumopathy.
  • Inability to perform Respiratory function test.

Treatment and study plan

Forced oscillation

Other

Primary outcomes

  1. Time difference in diagnosing distal airways functional disturbance by forced oscillation and by spirometry (standard methode).

    Time frame: 2 years

Sponsors and collaborators

Lead sponsor

Hopital Foch

Other

Registry information

Acronym: OSCILLOPOUMON

Important dates

Study start
2011
Primary completion
2015
Study completion
2015
First posted
Mar 8, 2013
Registry last updated
Jul 28, 2016

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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