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Sensory Mapping Following Video-assisted Thoracic Surgery

Conditions
Paresthesia
Dysesthesia
Pain
Registration Number
NCT01375283
Lead Sponsor
Rigshospitalet, Denmark
Brief Summary

This is a prospective observational cohort study on changes in sensory mapping.

Detailed Description

Not available

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
48
Inclusion Criteria
  • Age < 18 years old
  • Elective lung cancer surgery (VATS)
Exclusion Criteria
  • does not understand Danish
  • cognitive reduction
  • bilateral procedure planned
  • previous thoracic surgery
  • pregnant or nursing
  • known nerve affection from other cause
  • alcohol/substance abuse
  • inability to cooperate to pain scoring/sensory examination
  • > 5 mg methylprednisolone/day

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Area (cm2)3 months

Size of sensory dysfunction

Secondary Outcome Measures
NameTimeMethod
Pain3 months

pain intensity /numerical rating scale)

Trial Locations

Locations (1)

Section for Surgical Pathophysiology 4074

🇩🇰

Copenhagen, Denmark

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