None
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1.The subject is 18 years old or above, with no gender restrictions; 2.Subjects who require intradermal suture of surgical incision; 3.The subjects or their legal representatives are able to understand the research purpose and voluntarily sign the informed consent form.
Exclusion criteria
Exclusion criteria: 1.Subjects with non stage I suture incisions; 2.At any time before surgery, plasma glucose levels should be greater than 11.1mmol/L; 3.Subjects with systemic or local skin diseases near the surgical incision that may affect the evaluation of the surgical incision (including patients with scar constitution, herpes, and other skin diseases); 4.Patients with sepsis and/or systemic inflammatory response syndrome (SIRS) (diagnostic criteria for sepsis: significantly elevated total peripheral blood white blood cell count, reaching 10-30 × 10?/L; diagnostic criteria for systemic inflammatory response syndrome: body temperature>38.5 ° C, pathogen causing infection identified); 5.Pregnant and lactating women, those who plan to conceive during the trial period; 6.Researchers believe that individuals who are not suitable to participate in this clinical trial.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Grade A wound healing rate ; | — |
Secondary
| Measure | Time frame |
|---|---|
| Infection rate of superficial tissue in incisions;Pain Visual Simulation Score;Performance evaluation of instrument operation; | — |
Countries
China
Contacts
The Pearl River Hospital of Southern Medical University