Actively Recruiting
Reinnervated PAP Flap for Oral Cavity and Oropharyngeal Defect Reconstruction
Led by University Hospital, Basel, Switzerland · Updated on 2025-02-18
40
Participants Needed
1
Research Sites
191 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The aim of this study is to investigate sensory recovery and functional outcomes following oral cavity and oropharyngeal defect reconstruction with reinnervated PAP (profunda artery perforator) flaps.
CONDITIONS
Official Title
Reinnervated PAP Flap for Oral Cavity and Oropharyngeal Defect Reconstruction
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patient with defect involving the oral cavity or oropharynx who undergo reconstruction with a free reinnervated profunda artery perforator flap
You will not qualify if you...
- Younger than 18 years old
- Defect location other than the oral cavity or oropharynx
- Unable to give informed consent
- Unable to follow study procedures due to psychological disorders or dementia
- Unable or contraindicated to undergo the studied surgical intervention
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
University Hospital Basel
Basel, Switzerland, 4031
Actively Recruiting
Research Team
N
Nicole E. Speck, Dr. med.
CONTACT
D
Dirk J. Schaefer, Prof. Dr.
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
TREATMENT
Number of Arms
1
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