Post Operative Pain
Conditions
Brief summary
This is a prospective randomized study that included 60 patients and was divided into two equal groups of patients who were scheduled for LC, Ages 18 and 60 years, both sexes, ASA I-II and BMI 19 - 39. Group A received 30 ml levobupivacaine (0.25%) plus 3 mg morphine intraperitoneal at the site of surgery in the bed of the gallbladder via the navel port with the patient in a Trendelenburg position, Group B received 30 ml levobupivacaine (0.25%) plus 50 mg/kg magnesium sulfate in the same pattern as in the A group.
Interventions
DRUGintraperitoneal levobupivacaine and morphine
istillation of the peritoneum with levobupivacaine mixture with morphine
Sponsors
Sohag University
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)
Eligibility
Sex/Gender
ALL
Age
18 Years to 60 Years
Healthy volunteers
No
Inclusion criteria
* Patients who were scheduled for L.C, * Ages 18 and 60 years * ASA I-II and * BMI 19 - 39
Exclusion criteria
* Patients with hepatic or renal dysfunction * use of opioids 24 hrs prior to the study * treatment with steroids prior to surgery * drug or alcohol abuse, allergy to any of the study drugs * chronic pain syndrome as a result of neurological disease
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| reduction of postoperative pain | 8 hours | reduction of post operative visual analogue score |
Countries
Egypt
Outcome results
None listed