Evaluation of a Rehabilitation Program After Lung Surgery

This study has been completed.
Sponsor:
Information provided by (Responsible Party):
Hopital Foch
ClinicalTrials.gov Identifier:
NCT00969358
First received: August 28, 2009
Last updated: January 4, 2012
Last verified: January 2012
  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 ] [ Designated as safety issue: No ]

Secondary Outcome Measures:
  • Program Monitoring [ Time Frame: end of hospitalisation ] [ Designated as safety issue: No ]
  • postoperative complications [ Time Frame: end of hospitalisation ] [ Designated as safety issue: No ]

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

Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Both
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
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, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: 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

No publications provided

Responsible Party: Hopital Foch
ClinicalTrials.gov Identifier: NCT00969358     History of Changes
Other Study ID Numbers: 2009/12
Study First Received: August 28, 2009
Last Updated: January 4, 2012
Health Authority: France: Afssaps - Agence française de sécurité sanitaire des produits de santé (Saint-Denis)

ClinicalTrials.gov processed this record on October 21, 2014