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The Effect of Perioperative Lidocaine Infusion on Neutrophil Extracellular Trapping

T

The Catholic University of Korea

Status

Withdrawn

Conditions

Gastric Cancer

Treatments

Drug: normal saline
Drug: Lidocaine

Study type

Interventional

Funder types

Other

Identifiers

NCT04868747
NET-lidocaine-stomach cancer

Details and patient eligibility

About

To investigate the effect of perioperative lidocaine infusion on the neutrophil extracellular trapping after minimally invasive surgery for stomach cancer

Full description

To investigate the effect of perioperative lidocaine infusion on the neutrophil extracellular trapping, especially citrullinated histone3, neutrophil elastase, myeloperoxidase

Sex

All

Ages

20 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • diagnosis of stomach cancer
  • ASA class I-III
  • no metastatic disease

Exclusion criteria

  • hepatic, renal disease
  • chronic inflammatory disease, eg. rheumatoid arthritis
  • steroid or anti-inflammatory drug medication
  • allergies to study drugs
  • neuropsychiatric disease
  • refusal of participation
  • breast feeding or pregnancy
  • weight < 40 kg

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Quadruple Blind

0 participants in 2 patient groups, including a placebo group

study group
Experimental group
Description:
The study group receives the intravenous 1% lidocaine 1.5 mg/kg bolus followed by 1.5 mg/kg/h during surgery and 1.0 mg/kg/h until 24 hours after surgery (Max.\<120 mg/h).
Treatment:
Drug: Lidocaine
control group
Placebo Comparator group
Description:
The control group receives intravenous normal saline 0.15 ml/kg bolus followed by 0.15 ml/kg/h during surgery and 0.1 mg/kg/h until 24 hours after surgery.
Treatment:
Drug: normal saline

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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