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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00969358
Other study ID # 2009/12
Secondary ID
Status Completed
Phase N/A
First received August 28, 2009
Last updated September 22, 2016
Start date August 2009
Est. completion date December 2011

Study information

Verified date September 2016
Source Hopital Foch
Contact n/a
Is FDA regulated No
Health authority France: Afssaps - Agence française de sécurité sanitaire des produits de santé (Saint-Denis)
Study type Observational

Clinical Trial 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.


Recruitment information / eligibility

Status Completed
Enrollment 100
Est. completion date December 2011
Est. primary completion date December 2011
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility 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

Study Design

Observational Model: Cohort, Time Perspective: Prospective


Related Conditions & MeSH terms


Locations

Country Name City State
France Dept of Anesthesiology, Hôpital Foch Suresnes

Sponsors (1)

Lead Sponsor Collaborator
Hopital Foch

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary length of postoperative hospital stay end of hospitalisation No
Secondary Program Monitoring end of hospitalisation No
Secondary postoperative complications end of hospitalisation No
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