Patients with head and neck tumors
Conditions
Interventions
Experimental group:Supine position without occipitation during night sleep from the start of radiotherapy to 1 month after the end of radiotherapy
Control group:The same as conventional methods, such as the use of skin protectants, etc.
Sponsors
The First People’s Hospital of Lianyungang
Eligibility
Sex/Gender
All
Age
1 Years to 100 Years
Inclusion criteria
Inclusion criteria: 1.Patients with head and neck radiotherapy (radiotherapy dose >= 40 Gy);
Exclusion criteria
Exclusion criteria: 1.Excluding patients with radiotherapy dose <= 40 Gy;
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Incidence of grade II and above radioactive dermatitis; | — |
Secondary
| Measure | Time frame |
|---|---|
| Incidence of cervical skin pigmentation and grade I radiation dermatitis; | — |
Countries
China
Contacts
Public Contactzhangxueli
The First People’s Hospital of Lianyungang
Outcome results
None listed