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Comparing the topical effect of bupivacaine and hydrocortisone in gallbladder bed on post operative pain following laparoscopic cholecystectomy among chronic cholecystitis patients

Bupivacaine and hydrocortisone effect on post operative pain after laparoscopic cholecystectomy

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT2017012110222N7
Enrollment
90
Registered
2017-02-06
Start date
2017-03-21
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

cholelithiasis. Calculus of gallbladder with other cholecystitis

Interventions

Intervention 1: The first group receive 100 mg hydrocortisone topically during surgery . Intervention 2: The second group receive 10 mL of bupivacaine solution%.5 topically during surgery . Intervent
Treatment - Drugs
The first group receive 100 mg hydrocortisone topically during surgery .
The second group receive 10 mL of bupivacaine solution%.5 topically during surgery .
The Third group receive 10 cc of normal saline topically during surgery .

Sponsors

Vice chancellor for research of Shahrekord University of Medical Science
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Inclution criteria: Laparoscopic cholecystectomy due to symptomatic patients who were carrying Lithiasis Exclusion criteria: allergy to local anesthetics and drugs; morbid obesity; advanced respiratory diseases; Kidney disease; blood diseases; Liver disease; Cardiovascular disease; Chronic use of drugs, beta-adrenergic receptor antagonists; pregnant women; The mentally retarded

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Pain relief. Timepoint: 6 and 12 hours after surgery. Method of measurement: questionaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactBabak Alavi Farzane

Shahrekord University of Medical Sciences

alavi.b@skums.ac.ir+98 38 3222 0016

Outcome results

None listed

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