Swedish National Parotidectomy Study (SNaPs): Drainless Versus Standard Surgery
Recruiting
N/A
Interventional Study
Parotid Neoplasms
Post-operative Complications
Seroma as Procedural Complication
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
At a Glance
- Age
- 18 and older
- Sex
- Any
- Study type
- Interventional
- Purpose
- Health Services Research
- Participants needed
- 600 (estimated)
- Sponsor
- Uppsala University Hospital · Other
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About This Trial
The purpose of this study The purpose of this study is to find out if it is safe to perform surgery on the parotid gland (the large salivary gland in front of the ear) without using a wound drain. A wound drain is a small plastic tube used to remove excess fluid from the surgical site after the operation. Currently, using a drain is the standard practice in Sweden, which often means patients must …
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Patients scheduled to undergo partial or superficial parotidectomy without concurrent soft tissue surgery, in cases where a wound drain is traditionally used (extirpation of single adjacent lymph nodes is acceptable).
* ASA physical status class 1-3.
* Aged 18 years or older.
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Contacts