4DryField PH and Head and Neck Operations.
Enrolling by invitation · Not applicable
Conditions studied: Head and Neck
In brief
The aim of this study is to investigate whether 4DryField can reduce postoperative blood loss and drain duration following head and neck surgery. This is a prospective, single-blinded, randomized study that will recruit 60 patients without coagulopathy, not on anticoagulant therapy, and with no known allergy to 4DryField.
Key facts
- Study ID
- NCT07487636
- Run by
- Taichung Veterans General Hospital
- People needed
- 60
- Starts
- 2026-01-01
- Expected to finish
- 2026-12-31
- Last updated by the study team
- 2026-03-25
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Patients undergoing head and neck operations
You may not qualify if…
- Allergy to 4DryField
- Patients with coagulopathy
- Patients underwent head and neck radiotherapy
- Patients reluctant to join the study
- Patients who had carotid blowout
Where it is running
- Taichung Veterans General Hospital — Taichung, Taiwan, Taiwan
Full record on ClinicalTrials.gov
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