None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1) Patients aged 20 to 65 years old 2) Patients who consented to the study and obtained consent for the study 3) Patients planning to undergo thyroidectomy with an incision due to thyroid disease 4) Patients with no significant abnormal findings in laboratory and voice tests before surgery
Exclusion criteria
Exclusion criteria: 1) Patients judged to be inappropriate by the person in charge of the clinical trial 2) Take aspirin and antiplatelet drugs within 7 days of hospitalization 3) History of esophageal and airway related diseases 4) History of keloid or hypertrophic scar 5) Patients who participated in other clinical trials within 30 days 6) Patients scheduled to undergo lateral cervical lymph node resection 7) Patients who are clinically judged to have already formed adhesions after receiving frontal irradiation and surgery in the past 8) Patients with a history of allergies to drugs (especially Poloxamer, gelatin, chitosan, etc.)
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| effectiveness in anti-adhesion | — |
Secondary
| Measure | Time frame |
|---|---|
| safety | — |
Countries
Korea, Republic of
Contacts
Seoul National University Bundang Hospital