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Evaluation of a Rehabilitation Program After Lung Surgery

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
ClinicalTrials.gov Identifier: NCT00969358
Recruitment Status : Completed
First Posted : September 1, 2009
Last Update Posted : September 23, 2016
Sponsor:
Information provided by (Responsible Party):

Study Description
Brief Summary:
Fast track programs, multimodal therapy strategies, have been introduced in many surgical fields to minimize postoperative morbidity and mortality. This study is intended to evaluate a rehabilitation program in comparison with a historical series.

Condition or disease
Thoracic Surgery

Study Design

Study Type : Observational
Actual Enrollment : 100 participants
Observational Model: Cohort
Time Perspective: Prospective
Official Title: Evaluation of a Rehabilitation Program After Lung Surgery (Prospective Observational Study)
Study Start Date : August 2009
Primary Completion Date : December 2011
Study Completion Date : December 2011

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Rehabilitation
U.S. FDA Resources

Groups and Cohorts


Outcome Measures

Primary Outcome Measures :
  1. length of postoperative hospital stay [ Time Frame: end of hospitalisation ]

Secondary Outcome Measures :
  1. Program Monitoring [ Time Frame: end of hospitalisation ]
  2. postoperative complications [ Time Frame: end of hospitalisation ]

Eligibility Criteria

Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years and older   (Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population
tertiary care clinic
Criteria

Inclusion Criteria:

  • adult patient
  • ASA 1, 2 or 3
  • lung surgery (postero-lateral or axillary approach)
  • epidural analgesia

Exclusion Criteria:

  • preoperative oxygen therapy
  • lack of autonomy
  • unstable coronary artery disease
  • FEV1 < 50%
  • pregnancy
Contacts and Locations

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00969358


Locations
France
Dept of Anesthesiology, Hôpital Foch
Suresnes, France, 92150
Sponsors and Collaborators
Hopital Foch
Investigators
Study Chair: Marc Fischler, MD Hôpital Foch
More Information

Responsible Party: Hopital Foch
ClinicalTrials.gov Identifier: NCT00969358     History of Changes
Other Study ID Numbers: 2009/12
First Posted: September 1, 2009    Key Record Dates
Last Update Posted: September 23, 2016
Last Verified: September 2016