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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00834769
Other study ID # 2008/30
Secondary ID
Status Completed
Phase N/A
First received February 2, 2009
Last updated September 22, 2016
Start date December 2008
Est. completion date March 2009

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

Investigation of chronic pain frequency after thoracotomy for lung cancer. Risk factors for development of chronic pain are investigated. Questionnaire survey.


Recruitment information / eligibility

Status Completed
Enrollment 65
Est. completion date March 2009
Est. primary completion date March 2009
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- thoracotomized patients

Exclusion Criteria:

- mental incapacity,

- poor understanding of French,

- pre-existing chronic pain before surgery,

- redo-surgery

Study Design

Observational Model: Cohort, Time Perspective: Retrospective


Related Conditions & MeSH terms


Locations

Country Name City State
France Hopital 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 Pain and pain score one year postoperative No
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