Neuropathic in the Acute Post Operative Phase

Lung Cancer Clinical Trial

Official title:

Identification of Neuropathic Pain in the Acute Post Operative Phase Following Thoracotomy

Clinical Trial Details — Status: Terminated

Administrative data

• NCT number: NCT01300702
• Other study ID #: H4-2010-118#1
• Status: Terminated
• Phase: N/A
• First received: February 22, 2011
• Last updated: September 28, 2011
• Start date: February 2011
• Est. completion date: September 2011

Study information

• Verified date: September 2011
• Source: Rigshospitalet, Denmark
• Contact: n/a
• Is FDA regulated: No
• Health authority: Denmark: National Board of Health
• Study type: Observational

Clinical Trial Summary

Investigation of thermal thresholds and sensory mapping to thermal stimuli

Recruitment information / eligibility

• Status: Terminated
• Enrollment: 0
• Est. completion date: September 2011
• Est. primary completion date: September 2011
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• age > 18 years old

Exclusion Criteria:

• do not under stand Danish

• cognitive reduction

• previous thoracic surgery

• Pregnant or nursing

• inability to cooperate to pain scoring

Study Design

Observational Model: Cohort, Time Perspective: Prospective

Related Conditions & MeSH terms

• Lung Cancer

Locations

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

Sponsors (5)

Lead Sponsor	Collaborator
Rigshospitalet, Denmark	Innovative Medicines Initiative, Multidisciplinary Pain Centre, Section for Surgical Pathophysiology, Section of Acute Pain Management and Palliative Medicine

Country where clinical trial is conducted

Denmark, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Pain	pain intensity	14 days	No
Primary	quantitative sensory testing (QST)	thermal thresholds assesses via QST	14 days	No
Primary	Neuropathic pain	is the pain considered neuropathic	14 days	No