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Effect of varied dosage lidocaine on postoperative hyperalgesia

Effect of varied dosage lidocaine on postoperative hyperalgesia

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-IOR-17012406
Enrollment
Unknown
Registered
2017-08-18
Start date
2017-09-01
Completion date
Unknown
Last updated
2017-08-21

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

Conditions

fibroid

Interventions

Lidocaine group 1:Lidocaine 1.5mg/kg
Lidocaine group 2:Lidocaine 2.5mg/kg
Lidocaine group 3:Lidocaine 3.5mg/kg

Sponsors

The First Affiliated Hospital of Shihezi University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
20 Years to 60 Years

Inclusion criteria

Inclusion criteria: Body mass index (BMI) less than <30kg/m2, aged 20 to 60 years, ASA grade I or II, undergoing general anesthesia hysterectomy patients.

Exclusion criteria

Exclusion criteria: Liver, kidney function and respiratory dysfunction; mental illness; serious cardiovascular and cerebrovascular diseases; abnormal blood coagulation; opioid addiction history; any accident in operation patients were also excluded.

Design outcomes

Primary

MeasureTime frame
Dosage of lidocaine during operation;Preoperative pain threshold;postoperative pain threshold;—

Countries

China

Contacts

Public ContactDong Xiwei

The First Affiliated Hospital of Shihezi University

dede123@163.com+86 13899534304

Outcome results

None listed

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