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NCT01375283 Clinical Trial

Sensory Mapping Following Video-assisted Thoracic Surgery

Pain Clinical Trial

Official title:
Sensory Mapping Following Video-assisted Thoracic Surgery

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT01375283
Other study ID # H4-2010-118#2
Secondary ID
Status Recruiting
Phase N/A
First received June 15, 2011
Last updated January 4, 2012
Start date June 2011

Study information
Verified date January 2012
Source Rigshospitalet, Denmark
Contact Kim Wildgaard, MD
Phone +45 3545 3246
Email wildgaard@thoracotomy.eu
Is FDA regulated No
Health authority Denmark: Danish Board of Health
Study type Observational

Clinical Trial Summary

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

Recruitment information / eligibility
Status Recruiting
Enrollment 48
Est. completion date
Est. primary completion date August 2012
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility 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

Observational Model: Cohort, Time Perspective: Prospective

Related Conditions & MeSH terms

Locations
Country Name City State
Denmark Section for Surgical Pathophysiology 4074 Copenhagen

Sponsors (1)
Lead Sponsor Collaborator
Rigshospitalet, Denmark

Country where clinical trial is conducted

Denmark, 

Outcome
Type Measure Description Time frame Safety issue
Primary Area (cm2) Size of sensory dysfunction 3 months No
Secondary Pain pain intensity /numerical rating scale) 3 months No
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