Health Condition 1: K561- Intussusception Health Condition 2: O- Medical and Surgical
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Patients aged 18 or above who is undergoing abdominal surgery both elective and emergency through a midline laparotomy incision of length 15-25cm
Exclusion criteria
Exclusion criteria: Patients undergoing midline laparotomy due to trauma. Patients who had peritonitis. History of hypersensitivity or adverse reaction to the medications being used. Patients with chronic liver or renal disease History of previous midline laparotomy Body mass index greater than 30kg/m2 Those patients who did not give consent for study.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Pain was measured using a 0â??10 VAS (0 -no pain; 10-most severe pain) at 12 and 24hrs after surgery. A blinded physician instructed patients to rate their pain both at rest and with cough. The VAS for cough at 12 h after surgery was not done to avoid the most painful intervention of the study.Timepoint: Pain was measured using a 0â??10 VAS (0 -no pain; 10-most severe pain) at 12 and 24hrs after surgery. A blinded physician instructed patients to rate their pain both at rest and with cough. The VAS for cough at 12 h after surgery was not done to avoid the most painful intervention of the study. | — |
Secondary
| Measure | Time frame |
|---|---|
| Assessment of post surgical complication in paients.Timepoint: Relation between complications and post op pain | — |
Countries
India
Contacts
General Surgery