Skip to content

Effect of Intraoperative Intravenous lidocaine infusion And comparison with the effect of intravenous remifentanil infusion , on postoperative pain after laparoscopic cholecystectomy surgery

Effect of Intraoperative Intravenous lidocaine infusion And comparison with the effect of intravenous remifentanil infusion , on postoperative pain after laparoscopic cholecystectomy surgery

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20141009019470N89
Enrollment
81
Registered
2019-10-18
Start date
2019-11-06
Completion date
Unknown
Last updated
2019-11-05

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

Conditions

Acute cholecystitis. Calculus of gallbladder with acute cholecystitis

Interventions

Intervention 1: Intervention group: Immediately after endotracheal intubation, lidocaine 2% solution (1.5 mg / kg) will be administered slowly. Then lidocaine 2% infusion at 2 mg / kg dose will start

Sponsors

Shiraz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: ASA I-II Age 18 to 75 years Patients Candidate for Laparoscopic Cholecystectomy

Exclusion criteria

Exclusion criteria: Non-cooperation patients after surgery Severe physical and mental disorders Severe bradycardia (heart rate less than 40 times per minute) Severe bleeding leading to laparotomy A history of allergies to topical anesthetics and lidocaine and opioids Chronic use of opioids and nonsteroidal anti-inflammatory drug and alcohol Pregnancy History of heart, liver and kidney failure The heart rate is less than 50 minutes per minute and any block on the ECG

Design outcomes

Primary

MeasureTime frame
Severity of pain in recovery. Timepoint: On arrival to recovery and every 15 minutes to 60 minutes in recovery. Method of measurement: NRS.;Severity of pain in the ward. Timepoint: Every one hour up to 6 hours, and then 12 and 24 hours. Method of measurement: NRS.

Secondary

MeasureTime frame
Sedation Score. Timepoint: At the arrival to the recovery room. Method of measurement: four-point categorical scale.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAmir Javadi

Shiraz University of Medical Sciences

amir7093209@gmail.com+98 71 3647 4270

Outcome results

None listed

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