Applied Research of Surgical Pleth Index Combined with Anesthesia Depth Monitoring During Obstetrics and Gynecology Enhanced Recovery after Surgery

Status

Active, not recruiting

Phases

Phase 4

Study type

Observational

Source

ChiCTR

Registry ID

ChiCTR2200062284

Enrollment

Unknown

Registered

2022-07-31

Start date

2022-08-01

Completion date

Unknown

Last updated

2023-04-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

Experimental group:SPI and anesthesia depth monitoring

Control group:Routine monitoring

Eligibility

Sex/Gender

All

Age

22 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1. Aged from 22 to 60 years; 2. ASA I ~ II grade; 3. Patients suffering from gynecological diseases requiring surgery; 4. Approved by the Ethics Committee of the hospital, the patient agrees, voluntarily participates in the study and signs the informed consent.

Exclusion criteria

Exclusion criteria: 1. Patients with serious heart and lung disease or severe arrhythmia; 2. Patients with cardiac pacemaker implantation; 3. Long-term use of ß-blockers or ß-agonists; 4. Abuse of alcohol or psychotropic drugs; 5. Neuromuscular disease; 6. Those who are unable to act independently or refuse; 7. Patients with severe allergy or history of allergy to propofol; 8. Patients with malignant arrhythmia, cardiac arrest or postoperative difficulty in extubation who need to be admitted to ICU.

Design outcomes

Primary

Measure	Time frame
Surgical volumetric index (SPI);Anesthesia depth;Intraoperative vital signs;	—

Secondary

Measure	Time frame
Intraoperative abnormalities;Recovery from anesthesia;Complications;Postoperative recovery;	—

Countries

China

Contacts

Public ContactXu Tao

towerxutao@163.com+86 18918098660

Outcome results