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Evaluation of a Rehabilitation Program After Lung Surgery

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT00969358
First Posted: September 1, 2009
Last Update Posted: September 23, 2016
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.
Information provided by (Responsible Party):
Hopital Foch
  Purpose
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
Thoracic Surgery

Study Type: Observational
Study Design: Observational Model: Cohort
Time Perspective: Prospective
Official Title: Evaluation of a Rehabilitation Program After Lung Surgery (Prospective Observational Study)

Resource links provided by NLM:


Further study details as provided by Hopital Foch:

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

Secondary Outcome Measures:
  • Program Monitoring [ Time Frame: end of hospitalisation ]
  • postoperative complications [ Time Frame: end of hospitalisation ]

Enrollment: 100
Study Start Date: August 2009
Study Completion Date: December 2011
Primary Completion Date: December 2011 (Final data collection date for primary outcome measure)
  Eligibility

Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.


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 Submitted: August 28, 2009
First Posted: September 1, 2009
Last Update Posted: September 23, 2016
Last Verified: September 2016