Evaluation of adding intrathecal fentanyl and dexmedetomidine on postoperative analgesia
Phase 3
Recruiting
- Conditions
- ower limb sugary.Unspecified fracture of lower legS82.9
- Registration Number
- IRCT20110313006044N4
- Lead Sponsor
- Bandare-abbas University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 75
Inclusion Criteria
Addict patients with aged 18-65 years andASA II, I Candidate for lower limb orthopedic surgery under spinal anesthesia
Exclusion Criteria
Emergency surgeries
Patients with severe valvular heart disease
Patients with psychological disorders
Patients with a history of seizures
Patients with ASA > II
Patients with a history of allergy tothe drugs used
Patients with a ban on spinal anesthesia (coagulation problems, high ICP, sepsis, infection at the injection site)
Patients with neurological defects
Patients who fail the block and need to induce general anesthesia
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Postoperative analgesia. Timepoint: Patients' pain intensity is measured and recorded based on visual analog scale (VAS) in recovery during 2,4,6,12 hours after surgery. Method of measurement: Patients' severity of pain is based on the Visual Analogues Scale, with the left side indicating no pain and the right side showing the number 10 indicating the most severe pain. Score style 1-3 indicates mild pain, 4-7 moderate pain, severe pain 8-10), duration of analgesia from time to block until patient requests for analgesics.
- Secondary Outcome Measures
Name Time Method Side effects after surgery including nausea and vomiting and. Timepoint: During surgery and in recovery between 2,4,6,12 hours after surgery is measured and recorded. Method of measurement: Patient dissatisfaction.