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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02017834
Other study ID # UCENT005
Secondary ID
Status Completed
Phase N/A
First received January 31, 2012
Last updated December 1, 2014
Start date February 2012
Est. completion date November 2014

Study information

Verified date December 2013
Source University of Calgary
Contact n/a
Is FDA regulated No
Health authority Canada: Ethics Review Committee
Study type Interventional

Clinical Trial Summary

The harmonic scalpel is a tool that may reduce operative blood loss. Some studies also indicate it may result in faster surgery. A recently published randomized study from our group shows the harmonic scalpel reduces blood loss in neck dissection but it did not offer any reduction in OR time. The present study investigates the utility of the harmonic scalpel in resections involving removal of oral cavity tissues as well as the neck. Oral cavity resections are especially prone to blood loss and we believe the harmonic scalpel will confer benefits in this type of surgery, potentially reducing the need for blood transfusion.


Recruitment information / eligibility

Status Completed
Enrollment 36
Est. completion date November 2014
Est. primary completion date November 2014
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- age > 18 years

- oral cavity scc

- primary surgery including either uni or bilateral neck dissection (levels I-IV)

Exclusion Criteria:

- previous treatment for head and neck cancer

- unable or unwilling to give informed consent

- history of bleeding disorder

- other contraindications to surgery

Study Design

Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Single Blind (Subject), Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Procedure:
surgical resection
neck dissection and tumour resection will be performed either with or without the harmonic scalpel as an adjunct.

Locations

Country Name City State
Canada Foothills Hospital Calgary Alberta

Sponsors (1)

Lead Sponsor Collaborator
University of Calgary

Country where clinical trial is conducted

Canada, 

Outcome

Type Measure Description Time frame Safety issue
Primary blood loss intraoperative No
Secondary operating time intraoperative No