Pain control after open nephrectomy in donors. Other acute postprocedural pain
Conditions
Interventions
Intervention 1: Intervention Group 1: Erector Spinae (ESPB) Group. After confirming landmarks and the correct injection site (T7–T9 vertebral levels, erector spinae muscle, transverse process), an ult
Sponsors
Shahid Beheshti University of Medical Sciences
Eligibility
Sex/Gender
All
Age
18 Years to 70 Years
Inclusion criteria
Inclusion criteria: Elective open nephrectomy for kidney donor American Society of Anesthesiologists (ASA) physical status classification of I or II
Exclusion criteria
Exclusion criteria: Anticoagulant agent use Blood abnormality or coagulation disorders Allergy history to local anesthetics Patient refusal
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| First time to analgesic demand. Timepoint: First timepoint for requesting analgesic. Method of measurement: Minutes based on a stopwatch. | — |
Secondary
| Measure | Time frame |
|---|---|
| Total postoperative opioid consumption. Timepoint: Once after 24 hours after surgery. Method of measurement: The amount of opioid consumed by patients in the first 24 hours after surgery in milligrams (mg) and reported based on (Morphine Equivalent Dose - MED) from hospital medical records and data recorded in the PCA (Patient-Controlled Analgesia) pump.;Postoperative pain. Timepoint: The measurement will be taken postoperatively in the recovery room, and at 6, 12, and 24 hours after surgery. Method of measurement: Visual analog scale.;Number of times the patient requested analgesic medication. Timepoint: During the first 24 hours after surgery. Method of measurement: The number of times patients requested analgesic medication during the first 24 hours after surgery will be obtained from medical records. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactAlireza Shakeri
Shahid Beheshti University of Medical Sciences
Outcome results
None listed