Comparing the effects of adding dexmedetomidine to WALANT solution on onset, block duration, pain levels during and after surgery, and bleeding rate in distal radius fracture patients..
Conditions
Interventions
Intervention 1: Intervention group: Received Valant solution plus dexmedetomidine (20 ml 2% lidocaine, 2 CC 1000/01 epinephrine, 14 CC normal saline, 4 CC 8.4% sodium bicarbonate [total 40 CC], and 50
Sponsors
Shahid Beheshti University of Medical Sciences
Eligibility
Sex/Gender
All
Age
18 Years to 80 Years
Inclusion criteria
Inclusion criteria: Patients with distal radius fractures who are candidates for surgery
Exclusion criteria
Exclusion criteria: surgical site infection Peripheral vascular disease Severe anxiety lack of cooperation Needle phobia Coagulation disorders Ages under 18 or over 80 open fracture Fracture duration exceeding three weeks patient unwillingness to participate
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Time of onset of anesthesia. Timepoint: Prior to intervention. Method of measurement: hour.;Pain levels. Timepoint: Baseline (V1), 10 minutes post-injection (V2), incision (V3), gentle manipulation (V4), vigorous manipulation (V5), first drilling (V6), and postoperatively. Method of measurement: Visual Analog Scale score.;Sedation level. Timepoint: During surgery, during recovery, and 4 and 24 hours after surgery. Method of measurement: Richmond Agitation Sedation Scale.;Hand movement disability. Timepoint: 2 weeks, 1 month, 2 months, 3 months and 6 months after surgery. Method of measurement: QUICK DASH Test. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactMalihe Abniki
Shahid Beheshti University of Medical Sciences
Outcome results
None listed