Skip to content

Effects of cervical plexus block and perioperative intravenous infusion of lidocaine on postoperative recovery quality in patients undergoing thyroidectomy

Effects of cervical plexus block and perioperative intravenous infusion of lidocaine on postoperative recovery quality in patients undergoing thyroidectomy

Status
Recruiting
Phases
Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200065273
Enrollment
Unknown
Registered
2022-11-01
Start date
2022-11-01
Completion date
Unknown
Last updated
2023-05-15

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

Conditions

thyroid surgery

Interventions

Using neural monitoring,Cervical plexus block group:Take standardized steps for neuromonitoring,after anesthesia induction, in under the guidance of ultrasound with 0.375% pp paid 10 ml implement bila
Using neural monitoring,lidocaine group:Take standardized steps for neuromonitoring,lidocaine 1.5mg/kg was pumped intravenously before induction of anesthesia, followed by 1.5mg/kg/h intravenous infus
Using neural monitoring,saline control group:Take standardized steps for neuromonitoring,the intravenous infusion of normal saline was the same as that of lidocaine group and the use of normal saline
No nerve monitoring,Cervical plexus block group:No nerve monitoring ,after anesthesia induction, in under the guidance of ultrasound with 0.375% pp paid 10 ml implement bilateral neck shallow plexus n
No nerve monitoring,lidocaine group:No nerve monitoring,lidocaine 1.5mg/kg was pumped intravenously before induction of anesthesia, followed by 1.5mg/kg/h intravenous infusion until the end of surgery
No nerve monitoring,saline control group:No nerve monitoring,the intravenous infusion of normal saline was the same as that of lidocaine group and the use of normal saline was the same as that of cerv

Sponsors

The Affiliated Huaian Hospital of Xuzhou Medical University, Huai'an Second Hospital
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Patients undergoing thyroidectomy under general anesthesia 2.ASA ?-?; 3.Aged 18-65 years.

Exclusion criteria

Exclusion criteria: 1. Patients who do not sign informed consent; 2. Patients with heart, brain, lung, liver, kidney and other major organ diseases; 3. Patients with hypertension or hyperthyroidism; 4. The scope of operation was changed, thyroid resection or cervical lymph node dissection was not performed; 5. Patients with coagulation disorders or blood system diseases; 6. Allergic to lidocaine and other experimental drugs or adverse drug reactions, such as allergic reaction, poisoning reaction; 7. pregnant and lactating women; 8. surgical site or systemic infection; 9. Difficult airway during induction of anesthesia, and conventional intubation should be changed; 10. Patients refused to continue the trial.

Design outcomes

Primary

MeasureTime frame
QoR-40;SAS;SDS;PSQI;Nerve monitoring EMG signal parameters;

Countries

China

Contacts

Public ContactChenglan Xie

The Affiliated Huaian Hospital of Xuzhou Medical University, Huai'an Second Hospital

xiechenglan@163.com13776701556

Outcome results

None listed

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