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Clinical Trial Summary

The study will investigate characteristics of chronic pain after VATS surgery with two different sizes of videoscopic equipment.


Clinical Trial Description

n/a


Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Prevention


Related Conditions & MeSH terms


NCT number NCT00969423
Study type Interventional
Source Rigshospitalet, Denmark
Contact
Status Terminated
Phase N/A
Start date October 2009

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