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Can lidocaine infusion during laparoscopic surgery reduce the pain?

Evaluation of the effectiveness of intraoperative infusion of lidocaine on postoperative pain in laparoscopic cholecystectomy.

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT2013082110900N2
Enrollment
70
Registered
2013-09-22
Start date
2013-09-23
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Cholecystectomy. Cholecystitis

Interventions

Intervention 1: In intervention group Lidocaine (each ampoule contains 20 mg/ml Lidocaine, made by Daroopakhsh Co - Iran) with primary dose of 0.5 mg/kg and maintenance dose of 2 mg/kg/h is administer
Treatment - Drugs
Placebo
In intervention group Lidocaine (each ampoule contains 20 mg/ml Lidocaine, made by Daroopakhsh Co - Iran) with primary dose of 0.5 mg/kg and maintenance dose of 2 mg/kg/h is administered.
In control group placebo (normal saline) is administered.

Sponsors

Deputy of Research Kerman University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 85 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria are patient willingness to participation, ASA (American Society of Anesthesiologists) classification of I or II and elective laparoscopy. Exclusion criteria are history of sensitivity to local analgesics, long-lasting use of narcotics and steroids, pregnancy and history of cardiac or other chronic diseases and high blood pressure, age less than18 or more than 85, BMI more than 40, HR less than 50 and PR interval more than 0.2 sec. or any kind of cardiac block.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Pain. Timepoint: before and after operation. Method of measurement: Visual Analogue Scale (VAS).

Secondary

MeasureTime frame
Blood pressure. Timepoint: every 5 minutes and every 15 minutes in PACU. Method of measurement: digital monitoring device.;Heart Rate. Timepoint: every 5 minutes and every 15 minutes in PACU. Method of measurement: digital monitoring device.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactHssein Sattari

Kerman University of Medical Sciences

hosattari@gmail.com+98 34 1322 2250

Outcome results

None listed

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