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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01068457
Other study ID # VATS-hb2008-059
Secondary ID
Status Completed
Phase N/A
First received February 8, 2010
Last updated July 13, 2010
Start date December 2009

Study information

Verified date July 2010
Source Rigshospitalet, Denmark
Contact n/a
Is FDA regulated No
Health authority Denmark: National Board of HealthDenmark: The Danish National Committee on Biomedical Research Ethics
Study type Observational

Clinical Trial Summary

This is an explorative study investigating potential nerve injury after VATS.


Recruitment information / eligibility

Status Completed
Enrollment 48
Est. completion date
Est. primary completion date April 2010
Accepts healthy volunteers No
Gender Both
Age group 19 Years and older
Eligibility Inclusion Criteria:

- Able to understand and give consent

- Can read

- Residing in Denmark

Exclusion Criteria:

- Unable to understand the written information in Danish

- Abuse (Medicine, Drugs, Alcohol)

- Severe psychiatric Illness

- Conflicting neurological disease

Study Design

Observational Model: Cohort, Time Perspective: Retrospective


Locations

Country Name City State
Denmark Section for Surgical Pathophysiology 4074 andSection of Acute Pain management and Palliative Medicine. Copenhagen

Sponsors (1)

Lead Sponsor Collaborator
Rigshospitalet, Denmark

Country where clinical trial is conducted

Denmark, 

References & Publications (1)

Wildgaard K, Ravn J, Kehlet H. Chronic post-thoracotomy pain: a critical review of pathogenic mechanisms and strategies for prevention. Eur J Cardiothorac Surg. 2009 Jul;36(1):170-80. doi: 10.1016/j.ejcts.2009.02.005. Review. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Thresholds via QST Late postoperatively (3months) No
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