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The effectiveness of the NOX index on evaluating the plane of anesthesia for regional block under propofol anesthesia: a prospective, randomized, double-blind study

The effectiveness of the NOX index on evaluating the plane of anesthesia for regional block under propofol anesthesia: a prospective, randomized, double-blind study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2300075693
Enrollment
Unknown
Registered
2023-09-13
Start date
2023-09-13
Completion date
Unknown
Last updated
2023-09-18

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

Conditions

Diseases of limbs or lower abdomen requiring surgery

Interventions

A group:Firstly, data on the plane of anesthesia are obtained by patient self-report using intermittent mechanical stimulation with von-Frey filaments in the awake state. Then data on the plane of ane
B group:Firstly, data on the plane of anesthesia are obtained by the NOX index using intermittent mechanical stimulation with von-Frey filaments in the propofol-anesthetized state. Then data on the pl

Sponsors

The Third Xiangya Hospital of Central South University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1. Aged 18 to 60 years old; 2. Elective surgery to receive spinal anesthesia or brachial plexus block; 3. ASA class I-III; 4. BMI 18-28 kg/m2; 5. Volunteer to participate in this study and sign the written informed consent.

Exclusion criteria

Exclusion criteria: 1. Severe hepatic or renal dysfunction, or abnormal coagulation; 2. Central nervous system diseases such as intracranial hypertension; 3. Psychiatric diseases such as schizophrenia, mania or insanity; 4. Puncture site or systemic infection, etc; 5. Inability to cooperate during puncture, affecting the operation of puncture; 6. Long-term use of sedative or analgesic drugs 7. Those who are allergic or contraindicated to local anesthetics, fentanyl, propofol, lipid emulsions and benzodiazepines and their components; 8. Patients who are unable to accurately express the range and degree of pain; 9. Other conditions judged by the investigator to be unsuitable for enrollment.

Design outcomes

Primary

MeasureTime frame
Plane of anesthesia for regional block;

Secondary

MeasureTime frame
BISpro index;NOX index;VAS pain scores;Mean arterial pressure;Heart rate;

Countries

China

Contacts

Public ContactLiao Qin

The Third Xiangya Hospital of Central South University

xy3yyliaoqin@sina.com+86 137 8741 2348

Outcome results

None listed

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