The effect of sufentanil on intravenous anesthesia in orthopedic patients
Phase 3
Recruiting
- Conditions
- Forearm surgery.Unspecified fracture of forearmS52.9
- Registration Number
- IRCT20110313006044N3
- Lead Sponsor
- Bandare-abbas University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 60
Inclusion Criteria
All Candidates aged 18-50 years for- forearm surgery with ASA I,II classes
Exclusion Criteria
Patients who are allergic to sufentanil or topical anesthetic.
Patients with a history of liver or kidney disease.
Patients who have sickle cell anemia or convulsion.
Patients with Raynaud syndrome and neuropathy.
Patients who have uncontrolled hypertension and opioid addiction.
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Tourniquet pain. Timepoint: Pain intensity measurement at baseline (before intervention) and 5,10,15 and 20 min after injection. Method of measurement: Patients' severity of pain is based on the Visual Analogues Scale.;Quality of local anesthesia. Timepoint: During Surgery. Method of measurement: Numerical scale(1-4) of patient satisfaction.
- Secondary Outcome Measures
Name Time Method The evaluation of sensory block. Timepoint: During surgery every 10 minutes. Method of measurement: 22-gauge needle on palm in hypothenar (ulna nerve) and thenar (median nerve) eminences and back of the upper arm between thumb and forefinger (radial nerve).;The evaluation of motor block. Timepoint: During surgery every 10 minutes. Method of measurement: Observation.;Side effects such as nausea, vomiting, seizures, hypotension, bradycardia, and itching. Timepoint: During and after surgery. Method of measurement: Observation.