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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02928003
Other study ID # 2015/35
Secondary ID 2016-A00045-46
Status Completed
Phase N/A
First received
Last updated
Start date July 10, 2017
Est. completion date April 16, 2019

Study information

Verified date August 2019
Source Hopital Foch
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Chronic post-thoracotomy pain is the most common long-term complication that occurs after a thoracotomy with a reported incidence of up to 80%. Surgical approach as well as other factors (genetic, psychological) could have a major and independent role in the development of the post operative pain.The main objective of this study is to identify genetic and psychological profile (cognitive and emotional) of patients who develop chronic pain after lung surgery.


Recruitment information / eligibility

Status Completed
Enrollment 166
Est. completion date April 16, 2019
Est. primary completion date April 16, 2019
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Undergoing lung resection surgery.

- 18 years and older (without superior limit);

- Affiliated to french "securité sociale"

Exclusion Criteria:

- Emergency procedure

- litigation or search for compensation;

- Previous intervention in the same region;

- Peripheral neurological pathology (polyneuropathy) or central (brain damage, multiple sclerosis …) that may interfere with the evaluation of the post-operative pain

- Participation in another biomedical research protocol if there is an incompatibility with the present protocol.

- mental disability

- vulnerable person within the meaning of French law,

- poor understanding of French.

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Lung surgery
Genetic analysis and questionnaires

Locations

Country Name City State
France Institut Mutualiste Montsouris Paris
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 Number of patients with chronic pain 4 months after surgery 4 months
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