Microtia
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: (1) 6-12 years old; (2) Unilateral congenital microtia; (3) Simple microtia, not part of a syndrome; (4) Patients who underwent extubation and water injection in our hospital after operation; (5) Informed consent to this study.
Exclusion criteria
Exclusion criteria: (1) Patients with ear deformity caused by trauma, burns and other injuries; (2) After the dilator was taken out due to infection, the posterior auricular dilator was implanted again; (3) Patients with hemifacial short deformity or other deformities, or patients with microtia as part of other definite syndromes; (4) Patients with diseases affecting coagulation function, including but not limited to liver and kidney dysfunction, allergic purpura, idiopathic thrombocytopenic purpura and other hematological disorders; (5) Female patients in menstrual period, pregnancy and lactation; (6) Patients with any signs or symptoms of bacterial, viral, or fungal infection in the treatment area; (7) A history of keloid formation; (8) Patients with severe autoimmune diseases or systemic inflammatory diseases; (9) Patients with poor compliance who cannot be followed up for a long time.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| intraoperative blood loss;postoperative drainage; | — |
Secondary
| Measure | Time frame |
|---|---|
| postoperative surgical site pain; | — |
Countries
China
Contacts
Plastic Surgery Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College