Surgical pleth index guided analgsia in gynecologicai operations

Status

Recruiting

Phases

Early Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2100042507

Enrollment

Unknown

Registered

2021-01-22

Start date

2021-02-01

Completion date

Unknown

Last updated

2021-05-03

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

Conditions

Intraoperative analgsia in gynecologicai operations

Interventions

experimental group:Surgical pleth index guided analgsia

control group:Traditional monitoring

Eligibility

Sex/Gender

Female

Age

18 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1. ASA I - II patients; 2. Patients aged 18-60 years who are scheduled for surgery.

Exclusion criteria

Exclusion criteria: 1. Patients with severe cardiovascular disease, liver and kidney dysfunction, endocrine and neuropsychiatric diseases; 2. Patients with alcohol or drug abuse.

Design outcomes

Primary

Measure	Time frame
tracheal extubation time;Opioid dosage;VAS;	—

Countries

China

Contacts

Public ContactMinbo Fang

Li Huili Hospital of Ningbo Medical Center

fmb_1983@163.com+86 13819826972

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026