Labor analgesia
Conditions
Interventions
Wireless wearable monitoring group:Use wearable multi-parameter wireless monitoring devices
Traditional Guardianship Group:Use traditional wired monitoring equipment
Sponsors
Lishui Central Hospital
Eligibility
Sex/Gender
Female
Inclusion criteria
Inclusion criteria: 1.Expectant mothers; 2.Those who plan to undergo labor analgesia, voluntarily participate in this study and sign the informed consent form; 3.No severe heart or lung diseases, fetal distress or other underlying diseases that may affect the determination of monitoring results (ASA grade ?-?);
Exclusion criteria
Exclusion criteria: 1.There are contraindications for intraspinal block (such as coagulation disorders, intraspinal diseases, etc. 2.After assessment by an obstetrician, vaginal trial delivery is not possible (such as placenta previa, cephalopelphic disbalance, etc.); 3.There is an implantable heart device; 4.Suffering from severe or unstable mental or physical illness (ASA grade III-V); 5.Allergic to the attached electrode material, or having wounds or skin damage around the attached site; 6.Patients with infectious diseases (to ensure hygiene and safety); 7.Women who are transferred to cesarean section halfway due to various reasons; 8.Refuse to sign the informed consent form;
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Prognostic score of parturients;Neonatal score;Monitor the data drop rate;Accuracy of vital sign data;Duration of labor; | — |
Secondary
| Measure | Time frame |
|---|---|
| The working efficiency and satisfaction of medical staff;Maternal satisfaction; | — |
Countries
China
Contacts
Public ContactFang Zheng
Lishui Central Hospital
Outcome results
None listed