Status:
COMPLETED
Epidemiologic Multicentre Study of Neuropathic Post-surgical Pain
Lead Sponsor:
University Hospital, Clermont-Ferrand
Collaborating Sponsors:
Pfizer
Conditions:
Neuropathic Pain
Eligibility:
All Genders
18+ years
Brief Summary
This cohort study aims to know the prevalence at 3 and 6 months after surgery, of persistent pain, as well as to describe the neuropathic features of this pain. It includes more than 3000 patients sch...
Detailed Description
Neuropathic post-surgical pain (NPSP) motivates the consultation of the French Centres for Evaluation and Treatment of Pain in 20 to 35% of the cases. The following table shows the available data of l...
Eligibility Criteria
Inclusion
- Agreement to the study
- Scheduled for one of the following surgeries :
- caesarean section
- inguinal hernia repair
- mastectomy
- cholecystectomy under laparoscopy
- saphenectomy (excluding harvesting for coronary bypass)
- sternotomy
- thoracotomy
- knee arthroscopy
- Major over 18 years
Exclusion
- Emergency
- Inability to fill questionnaires
- Unreachable patients
Key Trial Info
Start Date :
April 1 2006
Trial Type :
OBSERVATIONAL
Allocation :
ACTUAL
End Date :
September 1 2011
Estimated Enrollment :
3322 Patients enrolled
Trial Details
Trial ID
NCT00812734
Start Date
April 1 2006
End Date
September 1 2011
Last Update
May 28 2019
Active Locations (1)
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1
CHU Clermont-Ferrand
Clermont-Ferrand, France, 63003