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The effect of washout of the surgery site with Marcaine or petedine on postoperative analgesia in patients with gallbladder

Effect of washout of the Cholecystectomy surgery site with Marcaine or pethidine solution on pain after laparoscopic cholecystectomy gallbladder surgery

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2017021632419N2
Enrollment
99
Registered
2017-04-04
Start date
2016-08-22
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

Gallstone. Occlusion of cystic duct or gallbladder without calculus

Interventions

Intervention 1: In the first group, then prepare to surgery and immediately after cholecystectomy and before removing the trocar, the liver washout will be performed with 1.5% mg per kg of Marcaine di
Treatment - Drugs
Placebo
In the first group, then prepare to surgery and immediately after cholecystectomy and before removing the trocar, the liver washout will be performed with 1.5% mg per kg of Marcaine diluted with 40 mL
In the second group, after the cholecystectomy, the liver washout will be performed with 0.5% mg per kg of pethedine diluted with 40 mL of saline normal.
In the third group will not make any infiltration.

Sponsors

Vice Chancellor for Research, Qazvin University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Inclusion criteria: a tendency to cooperate in the study and signed an informed consent form; Laparoscopic cholecystectomy surgery. Exclusion criteria: failure to discharge those with more than two days after Laparoscopic Cholecystectomy surgery; Marcaine or pethidine allergies; Class III and VI heart failure; Insufficiency of end Stage Renal Disease; Side effects of surgery; Open Cholecystectomy.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Pain score after after the cholecystectomy surgery. Timepoint: After entering the recovery, during times of 1, 2, 4, 8, 16, 24 and 48 hours after surgery. Method of measurement: The patient will be trained on how to measure.The postoperative pain will be measured using the visual analogue scale (VAS).

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr. Mohammad mahdi Khazravi

Qazvin University of Medical Science

mkh3526@gmail.com+98 28 3335 3064

Outcome results

None listed

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