NCT00969358

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.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
100

participants targeted

Target at P50-P75 for all trials

Timeline
Completed

Started Aug 2009

Typical duration for all trials

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

August 1, 2009

Completed
27 days until next milestone

First Submitted

Initial submission to the registry

August 28, 2009

Completed
4 days until next milestone

First Posted

Study publicly available on registry

September 1, 2009

Completed
2.2 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 1, 2011

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

December 1, 2011

Completed
Last Updated

September 23, 2016

Status Verified

September 1, 2016

Enrollment Period

2.3 years

First QC Date

August 28, 2009

Last Update Submit

September 22, 2016

Conditions

Thoracic Surgery

Outcome Measures

Primary Outcomes (1)

  • length of postoperative hospital stay

    end of hospitalisation

Secondary Outcomes (2)

  • Program Monitoring

    end of hospitalisation

  • postoperative complications

    end of hospitalisation

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

tertiary care clinic

You may qualify if:

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

You may not qualify if:

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

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Dept of Anesthesiology, Hôpital Foch

Suresnes, 92150, France

Location

Study Officials

  • Marc Fischler, MD

    Hôpital Foch

    STUDY CHAIR

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

August 28, 2009

First Posted

September 1, 2009

Study Start

August 1, 2009

Primary Completion

December 1, 2011

Study Completion

December 1, 2011

Last Updated

September 23, 2016

Record last verified: 2016-09

Locations

FR(1)