Condition 1: Postoperative Analgesia. Condition 2: Postoperative Analgesia. Acute pain Pain due to orthopedic internal implantation, fixation and other procedure
Conditions
Interventions
Intervention 1: After the written informed consent from the patients in the study the femoral block perform with guide of sonography and nerve stimulator on the lateral side of femoral artery below t
Treatment - Drugs
After the written informed consent from the patients in the study the femoral block perform with guide of sonography and nerve stimulator on the lateral side of femoral artery below the inguinal liga
Sponsors
Vice chancellor for research, Iran University of Medical Sciences
Eligibility
Sex/Gender
All
Age
18 Years to 65 Years
Inclusion criteria
Inclusion criteria: Inclusion criteria: Patients' consent? No usage of anti- coagulant drugs? No infection at the site of injection? Age between 18 and 65 years old? ASA1&2 Exclusion criteria: Patient refusal( no consent of the patients)? Surgery on PCL? Any complication due to injection or drugs, Calcium channel blocker usage, History of advanced renal disease? Allergy to drugs and Central or peripheral neurologic disorders.
Exclusion criteria
Exclusion criteria:
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Pain score. Timepoint: before block-just after block-3-6-12 hours after block. Method of measurement: visual analog scale. | — |
Secondary
| Measure | Time frame |
|---|---|
| Sedation. Timepoint: Just after block and 3-6-12 hours after block. Method of measurement: Sedation score.;Satisfication. Timepoint: Just after block and 3-6-12 houres after block. Method of measurement: Questionnare.;Additional requirement for opioid analgesics. Timepoint: Just after block and 3-6-12 hours after block. Method of measurement: Total dosage of injected additional analgesic in miligram. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactDr. Farnad Imani
Iran University of Medical Sciences
Outcome results
None listed