Reducing postoperative pain in laparotomy hysterectomy patients.
Conditions
Interventions
Intervention 1: The study units will be divided into three equal groups using a random sampling method and a random number table. In the first group, 10 cc of 0.25% bupivacaine will be injected into t
Sponsors
Hamedan University of Medical Sciences
Eligibility
Sex/Gender
Female
Age
40 Years to 65 Years
Inclusion criteria
Inclusion criteria: All female TAH candidates referring to Fatemieh Hamedan Medical Education Center The age range of patients is between 40 and 65 years old
Exclusion criteria
Exclusion criteria: Patients who were actively using opioids. All patients who refuse local anesthesia or for whom local anesthesia is prohibited, Surgery that has a special complication such as damage to internal organs during surgery. be accompanied by surgery other than TAH Surgery is more than 120 minutes or emergency surgery cancer
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Reduction of postoperative pain in laparotomy hysterectomy patients with bupivacaine injection. Timepoint: In the study to investigate the effect of bupivacaine injection in reducing the postoperative pain of laparotomy hysterectomy patients, the pain of the patients is measured within 2 to 4, 12 and 24 hours after the surgery. Method of measurement: Use Visual Analogue Scale. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactMaryam Ahmadi
Hamedan University of Medical Sciences
Outcome results
None listed