Tumescence in HNC Skin Graft Reconstruction
Head and Neck Cancer, Surgery--Complications, Graft Failure
About this trial
This is an interventional supportive care trial for Head and Neck Cancer
Eligibility Criteria
Inclusion Criteria Patients must meet all of the following criteria to be eligible for study entry.
- Ability to adhere to the study visit schedule and other protocol requirements.
- Men and women ≥18 years of age.
- Life expectancy ≥ 3 months.
- Planned surgery for head and neck cancer ablation requiring split-thickness skin grafting for reconstruction of free flap donor sites from the forearm and fibula.
Exclusion Criteria Patients who meet any of the following criteria will be excluded from study entry.
- Pregnant or lactating women.
- History of prior radiation.
- Any significant medical condition which, in the opinion of the investigator, will not be appropriate for the study.
- Severe infection that in the opinion of the investigator would interfere with patient safety or compliance on trial within 4 weeks prior to enrollment.
Sites / Locations
- UC Davis HealthRecruiting
Arms of the Study
Arm 1
Arm 2
Experimental
No Intervention
Tumescence During STSG Harvest
No Intervention
Prior to the split thickness skin graft (STSG) harvest, the tumescence technique will injection of 100-150 mL normal saline with 1:500,000 epinephrine injected into a deep dermal thigh tissue plane with 18-gauge spinal needle on a 60 mL syringe.
Patients randomized to "no tumescence" will have their free flap donor site reconstructed with a split thickness skin graft (STSG) harvested at 0.0175 inches using the dermatome to obtain a graft from the thigh.