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the effect of intraperitoneal lidocaineand bupivacain on post operative pain in laparoscopic cholecystectomy compare with normal saline in patient who are undergoing laparoscopic cholecystectomy .

the effect of intraperitoneal lidocaineand bupivacain on post operative pain in laparoscopic cholecystectomy compare with normal saline in patient who are undergoing laparoscopic cholecystectomy .

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2014020716516N1
Enrollment
168
Registered
2014-08-12
Start date
2014-03-21
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

Chronic cholecystitis. Chronic cholecystitis

Interventions

Intervention 1: 20 mL of lidocaine 1% was infused , and 20 mL of normal saline was infused intraperitoneally in Group A. Intervention 2: 20 mL of lidocaine 1% was infused intraperitoneally in Group B,
Treatment - Drugs
20 mL of lidocaine 1% was infused , and 20 mL of normal saline was infused intraperitoneally in Group A.
20 mL of lidocaine 1% was infused intraperitoneally in Group B,
20 mL of Bupivacain 0.25% was infused intraperitoneally in Group C

Sponsors

Lorestan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 70 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: patients that are candidate foe elective laparoscopic cholecystectomy; age between 20-70 years old. Exclusion criteria: the patients that have heart disease and hypertension and diabetes mellitus and chronic respiratory diseases.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Pain. Timepoint: 24 hours after surgery. Method of measurement: VAS score system.

Secondary

MeasureTime frame
Nausea and vomiting. Timepoint: Questionnaire. Method of measurement: 24 hours after surgery.;Blood pressure. Timepoint: Blood pressure measuring device. Method of measurement: 24 hours after surgery.;Pulse rate. Timepoint: 24 hours after surgery. Method of measurement: Pulse oximertry.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr. Sedigheh Nadri

Lorestan University of Medical Sciences

dr.s.nadri@lums.ac.ir+98 66 1323 6402

Outcome results

None listed

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