Clinical study on the effect of intravenous and inhalation anesthesia maintenance on the quality of the operative field during endoscopic nasal surgery

Status

Active, not recruiting

Phases

Early Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2100052259

Enrollment

Unknown

Registered

2021-10-24

Start date

2021-10-30

Completion date

Unknown

Last updated

2022-10-17

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

Conditions

Chronic nasosinusitis

Interventions

Intravenous anesthesia group:Total intravenous anesthesia

Inhalation anesthesia group:Inhaled anesthesia

Eligibility

Sex/Gender

All

Age

18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Patients who plan to undergo ESS under elective general anesthesia. 2. Aged 18-65 years, BMI (Body Mass Index) 18-35kg/m^2, ASA I-II grade. 3. Agree to participate in this study and sign the informed consent form before surgery.

Exclusion criteria

Exclusion criteria: 1. Severe ischemic heart disease, uncontrolled hypertension or asthma, liver and kidney dysfunction, use of platelet inhibitors or anticoagulant therapy, coagulation dysfunction and pregnancy. 2. Those with poor alignment of the laryngeal mask and/or air leakage pressure 1.2 or the platelet count and/or function abnormality was detected before surgery (platelet count 50 seconds).

Design outcomes

Primary

Measure	Time frame
Surgical field quality score;	—

Countries

China

Contacts

Public ContactDu Yingjie

Beijing Tongren Hospital Affiliated to Capital Medical University

duyingjiemazui@163.com+86 17602428628

Outcome results

None listed

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