se of Surgicel in Parotid Surgery
Not Applicable
- Conditions
- SialoceleSurgery - Other surgery
- Registration Number
- ACTRN12617000101381
- Lead Sponsor
- Gold Coast University Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot yet recruiting
- Sex
- All
- Target Recruitment
- 230
Inclusion Criteria
All patients undergoing a parotidectomy
Exclusion Criteria
Other procedures during the parotidectomy (neck dissection) and radical parotidectomies.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Sialocele formation which will be clinically diagnosed at the one week follow up outpatient appointment and confirmed and quantified on ultrasound[One week post surgery.]
- Secondary Outcome Measures
Name Time Method Drain output will be measured every 24hrs by direct observation of the drain bag by surgical staff caring for the patient and documented in the medical records.[Every 24 hours until drain removed];Length of hospital stay as determined by days in hospital since operation to discharge[Days in hospital from operation date to discharge date];Facial nerve palsy graded on the House-Brackmann scale from 1 to 5[Measured 2hrs, 24hrs and one week after operation]
Related Research Topics
Explore scientific publications, clinical data analysis, treatment approaches, and expert-compiled information related to the mechanisms and outcomes of this trial. Click any topic for comprehensive research insights.
What molecular mechanisms link Surgicel use to sialocele formation after parotidectomy?
How does Surgicel compare to fibrin sealants in reducing post-parotidectomy sialocele incidence?
Are there biomarkers predicting sialocele risk in patients undergoing parotid surgery with Surgicel?
What adverse events are associated with Surgicel in parotidectomy and how are they managed?
What hemostatic agents or surgical techniques are alternatives to Surgicel for parotidectomy outcomes?