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The Effect of Intravenous Lidocaine on Postoperative Fatigue Syndrome in Patients Undergoing Laparoscopic Radical Surgery For Colorectal Cancer

The Effect of Intravenous Lidocaine on Postoperative Fatigue Syndrome in Patients Undergoing Laparoscopic Radical Surgery For Colorectal Cancer - Effect of Intravenous Lidocaine On Redical Surgery For Colorectal Cancer

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400093973
Enrollment
Unknown
Registered
2024-12-15
Start date
2025-01-01
Completion date
Unknown
Last updated
2025-01-06

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

Conditions

Colorectal Cancer

Interventions

Lidocaine group:Lidocaine was given 1.5 mg/kg at the time of anesthesia induction, followed by 2 mg/kg/h pumping immediately until the end of the operation.
Blank control group:Conventional general anesthesia induction + equal volume normal saline + conventional anesthesia + intraoperative continuous pumping of equal volume normal saline

Sponsors

The Second Affiliated Hospital and Yuying Children's Hospital of Wenzhou Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1)Prior to the initiation of any trial-related activities, the subject shall obtain informed consent, fully understand the purpose and significance of the trial, and be willing to comply with the trial protocol; 2)18 years old to 75 years old; 3)The patients were classified as American Society of Anesthesiologists (ASA) grade I-III; 4)Patients undergoing laparoscopic radical surgery for colorectal cancer; 5)BMI:18 to 28 kg/m2.

Exclusion criteria

Exclusion criteria: 1)Weight less than 40kg; 2)History of local anesthetic allergy,such as lidocaine; 3)Preoperative fatigue; 4)Psychiatric and cognitive disorders and a history of epilepsy; 5)With cardiovascular disease (congenital heart disease, bradycardia, hypotension, heart block, etc.) 6)With a history of myasthenia gravis; 7)Participated in other clinical trials (received the experimental drug or placebo) within 3 months prior to surgery.

Design outcomes

Primary

MeasureTime frame
Identity consequence fatigue scale;Christensen fatigue score;

Secondary

MeasureTime frame
VAS pain score;CRP concentration;the number of times the analgesic pump is applied in the 48 hours after surgery ;The first time of the postoperative exhaust ;General information included age, sex ratio (male/female), body mass index (BMI), American Society of Anesthesiologists Anesthesia Rating (ASA), nutritional screening risk (NRS2002) score, preoperative albumin concentration, preoperative hemoglobin concentration,operation duration,and duration of anesthesia;The first time to get out of bed;Incidence of postoperative nausea and vomiting;Incidence of postoperative tinnitus;Incidence of postoperative numbness of lips ;

Countries

China

Contacts

Public ContactShangguan Wangning

The Second Affiliated Hospital and Yuying Children's Hospital of Wenzhou Medical University

sgwning@163.com+86 135 8763 7891

Outcome results

None listed

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