OSCILLOMOELL: Forced Oscillations for Diagnosis Help in Bronchiolitis Obliterans Syndrome in Post Bone Marrow Transplantation

Sponsor
Hopital Foch (Other)
Overall Status
Completed
CT.gov ID
NCT02902471
Collaborator
(none)
110
2
1
51
55
1.1

Study Details

Study Description

Brief Summary

A study to evaluate the role of forced oscillations in diagnosis of bronchiolitis obliterans syndrome in patients after bone marrow transplantation. The force oscillations technique will be compared with classical spirometry.

Condition or Disease Intervention/Treatment Phase
  • Other: Forced oscillations measure
N/A

Study Design

Study Type:
Interventional
Actual Enrollment :
110 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Diagnostic
Official Title:
Functional Evaluation of Distal Airways by Forced Oscillations: Diagnosis Help in Bronchiolitis Obliterans Syndrome in Post Bone Marrow Transplantation
Study Start Date :
Jun 1, 2011
Actual Primary Completion Date :
Sep 1, 2015
Actual Study Completion Date :
Sep 1, 2015

Arms and Interventions

Arm Intervention/Treatment
Experimental: Group A

Patients with bronchiolitis obliterans syndrome after bone marrow transplantation

Other: Forced oscillations measure

Outcome Measures

Primary Outcome Measures

  1. Number of days [2 years]

    Temporal difference between the date of the functional change measured by the technique of the forced oscillations and by the standard techniques of plethysmography.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Patients over 18 years

  • Bone marrow or hematopoietic stem cells transplantation for more than 100 days

  • Clinical stability

  • Patients affiliated to a social security system

  • Patients having given his (her) written consent.

Exclusion Criteria:
  • Bronchiolitis Obliterans already diagnosed

  • Unresolved Respiratory infection

  • Unresolved mechanical complication (pneumothorax, effusions)

  • Medicinal pneumopathy

  • Inability to perform pulmonary function tests

Contacts and Locations

Locations

Site City State Country Postal Code
1 CHRU de Lille Lille France
2 Hopital Foch Suresnes France 92150

Sponsors and Collaborators

  • Hopital Foch

Investigators

  • Principal Investigator: Jean-Louis Couderc, MD, PhD, Hopital Foch

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Hopital Foch
ClinicalTrials.gov Identifier:
NCT02902471
Other Study ID Numbers:
  • 2010/48
  • 2010-A01229-30
First Posted:
Sep 15, 2016
Last Update Posted:
Jul 16, 2018
Last Verified:
Apr 1, 2017
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jul 16, 2018