None
Conditions
Interventions
Trial Group:blunt suture needle
Control Group:Traditional round needle sutures
Sponsors
The Second Hospital of Anhui Medical University
Eligibility
Sex/Gender
Female
Inclusion criteria
Inclusion criteria: 1.cesarean section.
Exclusion criteria
Exclusion criteria: 1.known blood-borne infectious diseases such as hepatitis B, hepatitis C, HIV infection, or syphilis; 2.emergency operation at night (23:00-6:00 the next day) because the glove puncture and water injection test could not be carried out within 1 hour after the operation; 3.>2 doctors and >1 nurse participated in the operation; 4.the gloves were changed for other reasons than glove puncture during the operation; 5.Situations in which double gloves must be worn for operation.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary endpoint was the incidence of glove puncture among doctors and surgical nurses.; | — |
Secondary
| Measure | Time frame |
|---|---|
| Satisfaction of physicians;Blood-borne occupational exposure to needlestick injury;Incidence of poor healing of surgical incision; | — |
Countries
China
Contacts
Public ContactManRong Yu
Operating room,The Second Hospital of Anhui Medical University
Outcome results
None listed