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Effects of Perioperative Administration of Intravenous Lidocaine in Children Operated on for Acute Generalized Peritonitis

U

Université NAZI BONI

Status

Not yet enrolling

Conditions

Postoperative Pain

Treatments

Drug: Serum saline intravenous
Drug: Lidocaine intravenous

Study type

Interventional

Funder types

Other

Identifiers

NCT06051630
INSSA 3

Details and patient eligibility

About

Intravenous administration of lidocaine perioperatively after laparotomy for peritonitis could be an interesting alternative by reducing the duration of postoperative ileus, the intensity of pain and the patient's hospital stay, as well as the cost of management in our context of lack of financial, technical and human resources, hence the present study.

Enrollment

62 estimated patients

Sex

All

Ages

6 to 15 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • All patients aged 6 to 15, Classified according to the American Society of Anaesthesiologists (ASA) (I, II and III) admitted for peritonitis and whose parents have given informed consent

Exclusion criteria

  • State of shock
  • Severe renal insufficiency (creatinine clearance less than 30 ml/min)
  • History of allergy to lidocaine
  • Refusal to participate in the study

Trial design

Primary purpose

Other

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

62 participants in 2 patient groups, including a placebo group

Lidocaine group
Experimental group
Description:
The group will receive 1.5 mg/kg lidocaine 2% bolus, followed by a continuous electric syringe dose of 1.5 mg/kg/hour intraoperatively, then 1.5 mg/kg/hour during the first 24 hours postoperatively
Treatment:
Drug: Lidocaine intravenous
Saline group
Placebo Comparator group
Description:
The control group will receive an equivalent volume of saline: the volume of saline to be administered will be obtained by considering the dose of lidocaine 2% that the patient would have received if he/she had been in the interventional group.
Treatment:
Drug: Serum saline intravenous

Trial contacts and locations

0

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Central trial contact

Bertille KI, Doctor; Ismael GUIBLA, Doctor

Data sourced from clinicaltrials.gov

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