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Effect of intravenous lidocaine infusion on postoperative recovery of patients undergoing laparoscopic colorectal surgery

Effect of intravenous lidocaine infusion on postoperative recovery of patients undergoing laparoscopic colorectal surgery

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1900027635
Enrollment
Unknown
Registered
2019-11-22
Start date
2020-01-16
Completion date
Unknown
Last updated
2024-02-11

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

Conditions

Colorectal cancer

Interventions

Experimental group:Lidocaine will be infused intravenously, 1.5mg/kg for a single injection, and the continuous infusion volume will be 2mg / kg / h until the end of the operation
Control group:Saline

Sponsors

Fujian provincial hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. American Society of Anesthesiologists (ASA) grade I to ?; 2. Age > 18 years of age

Exclusion criteria

Exclusion criteria: 1. Severe arrhythmia; 2. Chronic opioid history; 3. Liver dysfunction; 4. Epilepsy and other diseases that may affect the study.

Design outcomes

Primary

MeasureTime frame
Quality of recovery;—

Secondary

MeasureTime frame
Postoperative acute pain score;Recovery of gastrointestinal function;Nausea, vomiting and other adverse reactions;Emergence time;Postoperative cumulative opioid consumption;—

Countries

China

Contacts

Public ContactYao Yusheng

Fujian Medical University

fjslyys@126.com+86 13559939629

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 7, 2026