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Efficacy of systemic lidocaine on quality of recovery in patients undergoing colorectal endoscopic submucosal dissection

Efficacy of systemic lidocaine on quality of recovery in patients undergoing colorectal endoscopic submucosal dissection

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100055030
Enrollment
Unknown
Registered
2021-12-30
Start date
2022-01-06
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

Colorectal precancerous lesions and early colorectal cancer

Interventions

lidocaine group:Patients received an intravenous bolus injection of lidocaine 1.5 mg/kg over 10 min before induction of anesthesia, followed by a continuous infusion of 2 mg/kg/h until the end of the
control group:Patients received a perioperative 0.9% saline infusion at the same rate as the lidocaine infusion.

Sponsors

Fujian Provincial Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Patients undergoing endoscopic colorectal mucosal dissection; 2. Aged >= 18 years; 3. American Society of Anesthesiologists (ASA) class 1 to 3.

Exclusion criteria

Exclusion criteria: 1. The patient refuses to participate; 2. BMI greater than 30; 3. Allergic or contraindication to study drugs; 4. History of chronic pain and long-term use of analgesic medication; 5. Severe arrhythmia; 6. Hepatic and renal dysfunction; 7. Any other conditions precluded study inclusion, such as cognitive impairment, pregnancy, or inability to communicate in Mandarin Chinese.

Design outcomes

Primary

MeasureTime frame
Incidence of postoperative cognitive recovery;

Secondary

MeasureTime frame
discharge time;propofol consumption;Incidence of overall recovery;patient's satisfiction;procedure time;the emergence time;Endoscopitst satisfaction;

Countries

China

Contacts

Public ContactHao Li

Fujian Provincial Hospital

fjslyys@126.com+86 13860636571

Outcome results

None listed

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