recruiting
Conditions
Interventions
group 1 placebo group (n=40): patients receive 40 ml of normal saline 0.9% will be streamed at the surgical site and the other half will be streamed into the coelomic cavity prior to deflation
grou
Sponsors
Mansoura university
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: morbidly obese patients undergoing laparascoic bariatric surgery whose body mass index >35 . ASA I and II.
Exclusion criteria
Exclusion criteria: patient refusal,neuromuscular diseases (as myopathies, myasthenia gravie),psychiatric, hepatic, renal and cardiac diseases,known intolerance to the study drugs or patients converted to open surgery.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| total analgesic requirements within 24 hours post operative | — |
Secondary
| Measure | Time frame |
|---|---|
| 1-changes in respiratory functions measurements within 24 hours postoperative 2-time to first analgesic request 3-visual analogue scale measurement of pain within 24 hours postoperative 4-any reported side effects as difficulty of breathing, nusea or vomiting 5-return of bowel function | — |
Countries
Africa
Contacts
Public Contactmohammed hegazy
Mansoura university anesthesia ans surgical intensive care department
Outcome results
None listed