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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT01300195
Other study ID # H4-2010-118#0
Secondary ID
Status Recruiting
Phase N/A
First received February 18, 2011
Last updated September 27, 2011
Start date February 2011
Est. completion date April 2013

Study information

Verified date September 2011
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

Prospective cohort study of factors predisposing to persistent post surgical pain after video-assisted thoracic surgery


Recruitment information / eligibility

Status Recruiting
Enrollment 200
Est. completion date April 2013
Est. primary completion date November 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:

- do 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 (5)

Lead Sponsor Collaborator
Rigshospitalet, Denmark all Blegdamsvej 9, 2100-Copenhagen, Denmark, Dept. of cardio-thoracic anaesthesia, Dept. of thoracic Surgery, Dept. Surgical PAthophysiology

Country where clinical trial is conducted

Denmark, 

Outcome

Type Measure Description Time frame Safety issue
Primary Persistent post surgical pain Pain intensity (Numerical Rating Scale) 3 months No
Primary Analgesic use type(s) and amount of analgesics used 3 months No
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