Comparison of intravenous Dexmedetomidine and Clonidine in change of ?hemodynamic parameter and block quality after spinal anesthesia with ?Ropivacaine in lower limb orthopedic surgery
Not Applicable
Recruiting
- Conditions
- Spinal.Other complications of anaesthesia
- Registration Number
- IRCT2017092020258N60
- Lead Sponsor
- Vice chancellor for research, Arak University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 120
Inclusion Criteria
18 to 60 years; ASA class I and II; both male and female; patients with lower limb orthopedic surgery
Exclusion criteria: Patient refusal to perform spinal anesthesia;?? failure to perform spinal anesthesia;?? ?body mass index more than 30??;?? history of the use of beta-blockers and alpha-2 ?agonists and calcium channel blockers;?? cardiovascular disease;?? pregnancy ?; ?coagulation disorders; localized infection in the spinal cord ;history of allergy to ?the drugs of dexmeditoimidine and clonidine and rupivacaine?;?? arrhythmia;?? ?psychological problems;?? peripheral and central homeopathy
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Blood pressure. Timepoint: Every 15 minute to end of surgery. Method of measurement: Barometer.;Heart rate. Timepoint: Every 5 minute to end of surgery. Method of measurement: Count.;Oxygen saturation. Timepoint: Every 15 minute to end of surgery. Method of measurement: Percent.;Sensory block. Timepoint: Every 1 minute. Method of measurement: Pin prick method ?.;Motor block. Timepoint: Every 5 minute. Method of measurement: Bromeg scale.;Pain. Timepoint: In recovery and 1 and 2 and 4 and 6 and 12 hours after surgery?. Method of measurement: Visual Analogue Scale.
- Secondary Outcome Measures
Name Time Method