Sensory Mapping and Thermal Thresholds After Thoracic Surgery

This study has been completed.

Sponsor:

Information provided by:

Rigshospitalet, Denmark

ClinicalTrials.gov Identifier:

NCT01274858

First received: January 10, 2011

Last updated: September 27, 2011

Last verified: February 2011

History of Changes

Tracking Information
First Received Date ^ICMJE	January 10, 2011
Last Updated Date	September 27, 2011
Start Date ^ICMJE	January 2011
Primary Completion Date	April 2011 (final data collection date for primary outcome measure)
Current Primary Outcome Measures ^ICMJE (submitted: February 2, 2011)	Thermal thresholds (Quantitative Sensory Testing [QST]) [ Time Frame: average 18 months after surgery ] [ Designated as safety issue: No ] Two QST with 10 days interval Sensory mapping [ Time Frame: average 18 months after surgery ] [ Designated as safety issue: No ] Two QST with 10 days interval
Original Primary Outcome Measures ^ICMJE (submitted: January 11, 2011)	Thermal thresholds (QST) [ Time Frame: average 18 months after surgery ] [ Designated as safety issue: No ] Sensory mapping [ Time Frame: average 18 months after surgery ] [ Designated as safety issue: No ]
Change History	Complete list of historical versions of study NCT01274858 on ClinicalTrials.gov Archive Site
Current Secondary Outcome Measures ^ICMJE	Not Provided
Original Secondary Outcome Measures ^ICMJE	Not Provided
Current Other Outcome Measures ^ICMJE	Not Provided
Original Other Outcome Measures ^ICMJE	Not Provided

Descriptive Information
Brief Title ^ICMJE	Sensory Mapping and Thermal Thresholds After Thoracic Surgery
Official Title ^ICMJE	Sensory Mapping and Thermal Thresholds After Thoracic Surgery
Brief Summary	The study will investigate topography of sensory changes late after lung cancer surgery
Detailed Description	Not Provided
Study Type ^ICMJE	Observational
Study Design ^ICMJE	Observational Model: Cohort Time Perspective: Retrospective
Target Follow-Up Duration	Not Provided
Biospecimen	Not Provided
Sampling Method	Non-Probability Sample
Study Population	Lung cancer patients
Condition ^ICMJE	Lung Cancer
Intervention ^ICMJE	Not Provided
Study Group/Cohort (s)	lung cancer surgery
Publications *	Not Provided
* Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.

Recruitment Information
Recruitment Status ^ICMJE	Completed
Estimated Enrollment ^ICMJE	12
Completion Date	April 2011
Primary Completion Date	April 2011 (final data collection date for primary outcome measure)
Eligibility Criteria ^ICMJE	Inclusion Criteria: Understand Danish Age > 18 years old PTPS Exclusion Criteria: Cognitive dysfunction Repeated thoracic surgery Nerve injury from other causes Drug or alcohol abuse
Gender	Both
Ages	18 Years and older
Accepts Healthy Volunteers	No
Contacts ^ICMJE	Contact information is only displayed when the study is recruiting subjects
Location Countries ^ICMJE	Denmark

Administrative Information
NCT Number ^ICMJE	NCT01274858
Other Study ID Numbers ^ICMJE	H-B-2008-059/6
Has Data Monitoring Committee	No
Responsible Party	MD, Kim Wildgaard, Section for Surgical Pathophysiology 4074
Study Sponsor ^ICMJE	Rigshospitalet, Denmark
Collaborators ^ICMJE	Not Provided
Investigators ^ICMJE	Not Provided
Information Provided By	Rigshospitalet, Denmark
Verification Date	February 2011
^ICMJE Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP

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