Postoperative Pain. Acute pain, not elsewhere classified
Conditions
Interventions
Intervention 1: Intervention group: In this group, a pain pump containing 100 cc of normal saline and 0.5 micrograms/kg of Remifentanil 2mg manufactured by Elixir Company of Iran will be installed in
Sponsors
Arak University of Medical Sciences
Eligibility
Sex/Gender
All
Age
18 Years to 65 Years
Inclusion criteria
Inclusion criteria: Candidates for emergency laparotomy include cancer of abdominal organs, peritonitis, appendicitis, pancreatitis, abscess, adhesions (after trauma or surgery), diverticulitis, intestinal perforation or obstruction, foreign bodies and internal bleeding in accessible spaces. Aged 18 to 65 years Consent of the participants to participate in the study
Exclusion criteria
Exclusion criteria: Addiction to any drug Known hypersensitivity to remifentanil or Apotel Complicated laparotomy Laparotomy with long unconventional time Wound infection
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Intensity of pain. Timepoint: Immediately after consciousness, 1 hour later, 3 hours later, 8 hours later and finally 24 hours after surgery. Method of measurement: Visual analog scale.;Taking additional painkillers. Timepoint: Within 24 hours after surgery. Method of measurement: History.;Side effects. Timepoint: during operation. Method of measurement: History. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactDr. Alireza Kamali
Arak University of Medical Sciences
Outcome results
None listed