Perioperative sleep outcome
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: ? Gender unlimited ? Age 18-75 years old, 18 = BMI = 28Kg/? ? ASA Level I-III ? Patients who require thoracoscopic lobectomy (including partial lobectomy and segmental resection) and are hospitalized ? Having basic reading and comprehension skills, or clear Q&A skills, able to complete scale surveys with the help of medical staff. ? Sign an informed consent form, voluntarily participate in this project and be able to complete it as requiredClose monitoring of patients
Exclusion criteria
Exclusion criteria: ? Existence of mental disorders such as anxiety and depression, as well as other neurological disorders ? Patients with planetary ganglion block, including coagulation dysfunction, local skin infection, thyroid enlargement, and abnormal cardiac excitation conduction, are prohibited ? Patients who are unable to cooperate or persist in treatment, and anticipate poor compliance ? The patient is also participating in other clinical trial studies ? Any researcher deemed unsuitable to participate in this experiment due to other reasons
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Insomnia Severity Index(ISI)); | — |
Secondary
| Measure | Time frame |
|---|---|
| Pittsburgh sleep quality index(PSQI));Self-Rating Scale of Sleep;Deep sleep duration;Light sleep time;Rem sleep time;Visual analog scoring(VAS);The incidence of major postoperative complications;Length of stay(LOS); | — |
Countries
China
Contacts
The First Affiliated Hospital of Anhui Medical University